Boston Scientific Corporation (NYSE:BSX) Q4 2023 Earnings Call Transcript

Boston Scientific Corporation (NYSE:BSX) Q4 2023 Earnings Call Transcript January 31, 2024

Boston Scientific Corporation beats earnings expectations. Reported EPS is $0.55, expectations were $0.51. BSX isn’t one of the 30 most popular stocks among hedge funds at the end of the third quarter (see the details here).

Operator: Good morning and welcome to the Boston Scientific Fourth Quarter 2023 Earnings Call. All participants will be in listen-only mode. [Operator Instructions] After today’s presentation, there will be an opportunity to ask questions. [Operator Instructions] Please note this event is being recorded. I would now like to turn the conference over to Lauren Tengler, Vice President, Investor Relations. Please go ahead.

Lauren Tengler: Thank you, Drew. Welcome, everyone, and thanks for joining us today. With me on today’s call are Mike Mahoney, Chairman and Chief Executive Officer; and Dan Brennan, Executive Vice President and Chief Financial Officer. We issued a press release earlier this morning announcing our Q4 and full year 2023 results, which included reconciliations of the non-GAAP measures used in the release. We have posted a copy of that release, as well as reconciliations of the non-GAAP measures used in today’s call to the Investor Relations section of our website under the heading Financials & Filings. The duration of this morning’s call will be approximately one hour. Mike and Dan will provide comments on Q4 and full year performance, as well as the outlook for the business including 2024 guidance, and then we’ll take your questions.

During today’s Q&A session, Mike and Dan will be joined by our Chief Medical Officer, Dr. Ken Stein. Before we begin, I’d like to remind everyone that on this call, operational revenue growth, excludes the impact of foreign currency fluctuations, and organic revenue growth further excludes acquisitions and divestitures for which there are less than a full period of comparable net sales. Relevant acquisitions and divestitures excluded for organic growth are Baylis Medical, which closed on February 14th, 2022; the majority stake investment in Acotec Scientific Holdings Limited, Apollo Endosurgery and Relievant Medical, which closed in February, April, November 2023, respectively. Divestitures include the Endoscopy Pathology business, which closed in April 2023.

Guidance excludes the previously announced agreement to acquire Axonics, Inc., which is expected to close in the first half of 2024, subject to customary closing conditions. For more information, please refer to our financial and operating highlights deck, which may be found on our Investor Relations website. On this call, all references to sales and revenue, unless otherwise specified, are organic. This call contains forward-looking statements within the meaning of federal securities laws, which may be identified by words like anticipate, expect, may, believe, estimate, and other similar words. They include among other things, statements about our growth in market share, new and anticipated product approvals and launches, acquisitions, clinical trials, cost savings and growth opportunities, our cash flow and expected use, our financial performance, including sales, margins and earnings as well as our tax rates, R&D spend and other expenses.

If our underlying assumptions turn out to be incorrect, or if certain risks or uncertainties materialize, actual results could vary materially from the expectations and projections expressed or implied by our forward-looking statements. Factors that may cause such differences include those described in the Risk Factors section of our most recent 10-K and subsequent 10-Qs filed with the SEC. These statements speak only as of today’s date and we disclaim any intention or obligation to update them. At this point, I’ll turn it over to Mike.

Michael Mahoney: Thanks, Lauren, and thank you to everyone for joining us today. 2023 results were excellent, and our global performance represented one of the strongest years in company history, exceeding our financial goals that we set for the year. This performance is fueled by innovation and clinical evidence generation, commercial execution, and the winning spirit of our global teams. In fourth quarter ’23, total company operational sales grew 15%. Our organic sales grew 14% versus fourth quarter ’22, exceeding the high end of our guidance range of 8% to 10%. Full-year ’23 operational sales growth of 13% versus 2022, while organic sales grew 12%, exceeding our guidance of approximately 11% for the full year. Importantly, six of our eight business units grew sales double-digit in the fourth quarter and double-digits for the full year 2023.

And all of our regions also grew double-digits in the fourth quarter and double-digits full year 2023. This performance is a testament to our category leadership strategy and our focus on innovation bolstered by commercial excellence. Fourth quarter adjusted EPS at $0.55 grew 24% versus 2022, exceeding the high end of our guidance range of $0.49 to $0.52. Full year adjusted EPS of $2.05, grew 20% versus 2022, also exceeding the high end of our guidance range of $1.99 to $2.02. Q4 adjusted operating margin was 26.6% and full year ’23 was 26.3%, which is exciting because it exceeds pre-pandemic levels. We generated a full year cash flow of $1.8 billion and adjusted free cash flow of $2.5 billion in line with our expectations. Now for our 2024 outlook.

We expect healthy procedure volumes to continue and our guidance to organic growth of seven to nine for the first quarter of ’24, and eight to nine for the full year of 2024. Our Q1’24 adjusted EPS estimate is $0.50 to $0.52. We expect our full year adjusted EPS to be $2.23 to $2.27, representing growth of 9% to 11%. This guidance excludes the acquisition of Axonics, which is expected to close in the first half of ’24. Despite pressures on margins in ’24 from FX headwinds, as well as investments in manufacturing capacity and selling expenses to fuel our exciting launches, we remain committed to improving operating income margins in 2024 and to our goal of improving adjusted operating margin by 150 basis points in ’24 to ’26. Now, Dan will provide more details on those financials for both 2023 and 2024.

I’ll now provide additional highlights on ’23 results along with comments on our outlook. Regionally on an operational basis, the US grew 11% for the fourth quarter of ’22. Full year 2023 grew 10% with particular strength in our Watchman, EP, Endo and Uro business units. Europe, Middle East and Africa grew 12% on an operational basis versus Q4 ’22 and 13% on a full year basis. This above-market growth is supported by new and ongoing product launches across the portfolio, price discipline and strong commercial execution. We’re excited about the year ahead with ongoing momentum across the region, particularly with our innovative EP portfolio and further opportunity in our growth in emerging markets within the EMEA region. Asia Pacific grew 17% operationally versus Q1 in ’19 versus the full year 2022 with all major markets growing strong double-digits.

Japan had a strong year growing double-digits for ’22 with ongoing momentum from new products, most notably AGENT, DCB, Rezūm, POLARx FIT and WATCHMAN FLX. And on a full-year basis, China grew approximately 20% versus 2022. This consistent growth is fueled by the diverse portfolio, focus on innovation and strong commercial execution. Looking ahead, we expect China to be an accretive mid-teens grower over our ’24 to ’26 LRP. And to achieve over $1 billion in sales in ’24, supported by new product launches, supply chain agility and sustained investments in our talents and capabilities. The team Latin America grew 17% operationally versus both Q4 and full year ’22, with seven of eight business units growing double-digits on a full year basis.

I’ll now provide some additional commentary on our BUs. Urology had an excellent quarter, 10% organic growth versus Q4 ’22, and on a full year basis grew 11% organically. Full year growth was led by our Stone Management and Prosthetic Urology globally. And in 2023, we re-launched our direct-to-patient campaign driving therapy awareness for erectile dysfunction and supporting double-digit growth within our Prosthetic Urology franchise. We’re excited about the opportunities ahead in Urology, including our recently announced agreement to acquire Axonics, a medical technology company that offers innovative devices, treat urinary and bowel dysfunction. We look forward to bringing these complementary portfolios together and expanding access to differentiated technologies for physicians and patients.

Endoscopy sales were also excellent in the quarter, growing 12% operationally and 11% organically versus fourth quarter of ’22, on a full year basis, growing 12% operationally and 11% organically. Within the quarter, strong results were led by AXIOS and single-use scopes, both growing double-digits. On a full year basis, all regions grew double-digits, supported by the broad and deep portfolio, new product innovation and focus on commercial excellence. Neuromodulation sales grew 7% operationally and 3% organically versus fourth quarter ’22, on a full-year basis, 7% operationally and 5% organically versus ’22. Our Brain franchise grew double-digits both in the quarter and on a full-year basis, driven by the Vercise Genus portfolio and our innovative Image Guided Programming, which is designed to improve the precision and efficiency of the deep brain stimulation procedure.

In the fourth quarter, on an organic basis, our Pain franchise was flat year-over-year, which was in line with our expectations. We expect our performance to improve in 2024 with the recent launch of our US WaveWriter Alpha DPN indication and the strong and real-world data on FAST recently presented at NANS. Furthermore, with the completion of our Relievant Medsystems acquisition in the fourth quarter, we’re excited about our ability to offer an expanded Pain portfolio that supports a comprehensive treatment algorithm now included a novel Intracept system for the treatment of chronic low back pain. Peripheral Interventions sales were excellent, also growing 12% operationally and 10% organically versus Q4, on a full-year basis, growing 13% operationally and 11% organically versus ’22.

Arterial growth was led by the performance of our Drug-Eluting portfolio both in Q4 and on a full year. This market remains underpenetrated with more than half the procedure is still being used with bare-metal devices, underscoring the importance of our ongoing commitment to innovation and clinical evidence. In Venous, Q4 and full year growth was led by Varithena, our market-leading varicose vein technology. Additionally, in fourth quarter, EKOS growth was supported by REAL-PE, the largest real-world and near real-time dataset evaluating advanced therapies for pulmonary embolism patients. Our Interventional Oncology franchise performed extremely well in the fourth quarter and in 2023, growing low double-digits with strength across our portfolio of robust embolization technologies and cancer therapies We continue to look to expand our clinical evidence and are pleased to have commenced enrollment in the ROWAN trial, which will assess the safety and efficacy of using TheraSphere in combination with immunotherapy to treat HCC, the most common type of primary liver cancer.

Cardiology delivered tremendous quarter — delivered tremendous fourth quarter and year with both operational and organic sales growing 14% versus fourth quarter and for the full year 2022. Within Cardiology, Interventional Cardiology Therapies sales grew 10% for the full year and — for the fourth quarter and full year. On a full-year basis, the Coronary Therapies franchise growth was driven by strong performance in our international regions and our Imaging franchise globally. AGENT Drug-Coated Balloon continues to perform very well in Japan. We now expect approval of AGENT in the US in the first half of 2024. AGENT DCB will be the first coronary drug-eluting balloon in the US indicated for in-stent restenosis, providing physicians and their patients a solution for this unmet clinical need.

Our Structural Heart Valves franchise grew double-digits in both fourth quarter and in a full year basis, led by the performance of ACURATE Neo2 in Europe. And we now have treated more than 70,000 patients to date with our ACURATE technology globally. As we look ahead, we anticipate approval of ACURATE Prime in Europe in 2025. However, after reviewing a planned interim analysis of the US ACURATE IDE data, we will now wait for the full one-year data from the RCT cohort of 100 patients to determine our regulatory strategy. Therefore, we no longer anticipate the approval of ACURATE Prime in the US in 2024. Additionally in alignment with the FDA, we are suspending enrollment in the Single-arm Continued Access study, while continuing to enroll in the randomized extended durability cohorts.

We expect to have more information in the second half of 2024, following the full data review. WATCHMAN sales grew 23% organically versus fourth quarter ’22 and 25% on a full year basis. Q4 finished with record sales and strong utilization in all major markets. We have now treated over 400,000 patients globally with the WATCHMAN technology. US Q4 growth of 23% was supported by the breadth of the portfolio and the initial launch of WATCHMAN FLX Pro, which we expect to move into full launch in the first quarter. We continue to expand the breadth of clinical evidence supporting this technology and are pleased with the pace of enrollment within our post-market HEAL-LAA trial, including our newly added cohort, which is studying WATCHMAN FLX Pro, an underrepresented patient population.

We also look forward to initiating our Monotherapy trial, SIMPLIFY trial later this year, which will study WATCHMAN FLX Pro with the simplified post-implant drug regimen. Cardiac Rhythm Management sales grew 5% organically versus Q4 ’22, and on a full year basis grew 6% organically versus ’22. On a full year basis, our Diagnostics franchise grew double-digits outpacing market growth, driven by broad portfolio and ongoing investments in innovation. In Core CRM, in both fourth quarter and on a full year basis, our high-voltage business grew low-single digits and our low-voltage business grew mid-single-digits. 2023 performance was driven by our differentiated high-voltage portfolio and shock polarity options. As we look ahead, we expect our Core CRM growth to be in line with the market performance in ’24.

Turning to Electrophysiology, sales grew 43%, both operationally and organically versus fourth quarter ’22, and on a full year basis grew 37% operationally and 33% organically versus ’22. US fourth quarter sales grew 40% organically, driven by our POLARx launch and ongoing momentum with our Access Solutions portfolio. Our international EP growth accelerated in the fourth quarter, growing 46% organically, fueled by improved FARAPULSE console supply. We now treated over 40,000 patients globally with the FARAPULSE technology to-date. And with the news this morning that we received FDA approval for FARAPULSE, we are thrilled to enter the US market immediately. We continue to invest in ClinicalEVIDENCE to study new indications and support access to our FARAPULSE technology.

Late last year, we initiated the AVANT GUARD trial to evaluate the safety and efficacy of the system. It’s a first-line treatment for Persistent AF compared to antiarrhythmic drug therapy. Additionally, real-world data was presented at AHA for more than 17,000 patients treated with the FARAPULSE from the MANIFEST-17K registry, which reinforced the real-world safety profile of the FARAPULSE platform with no reports of permanent phrenic nerve palsy or pulmonary vein stenosis or esophageal injury and an overall major adverse rate event rate of less than 1%. We’re excited to bring this innovative technology to more markets and expect approval of FARAPULSE in Japan — China and Japan likely in the second half of this year. In closing, I’m very proud of our global team what we were able to accomplish in ’23, resulting in a full year organic sales growth of 12% and adjusted EPS growth of 20%.

We’re excited about the year ahead and remain focused on our talent, sustaining a culture that’s motivated to drive differentiated performance and achieve our long-range plan goals. Those goals, as a reminder, are sales an average of 8% to 10% over the three-year period, while expanding adjusted operating margin by 150 basis points, including double-digit adjusted EPS growth, an improvement of our free cash flow conversion to approximately 70% in 2026. With all of that, I’ll pass it over to Dan to provide more details on the financials.

Daniel Brennan: Thanks, Mike. Fourth quarter 2023 consolidated revenue of $3,725 million, represents 14.9% reported growth versus fourth quarter of 2022 and includes a 40 basis point tailwind from foreign exchange, in line with our expectations. Excluding this $12 million tailwind from foreign exchange, operational revenue growth was 14.5% in the quarter. Sales from closed acquisitions and divestitures contributed 90 basis points resulting in 13.6% organic revenue growth, exceeding our guidance range of 8% to 10%. Q4 2023 adjusted earnings per share of $0.55 grew 24% versus 2022, exceeding the high-end of our guidance range of $0.49 to $0.52, primarily driven by our strong sales performance. Full year 2023 consolidated revenue of $14,240 million represents 12.3% reported revenue growth versus full year 2022 and includes an 80 basis point headwind from foreign exchange, again in line with our expectations.

Excluding this $104 million headwind from foreign exchange, operational revenue growth for the year was 13.1%. Sales from closed acquisitions and divestitures contributed 80 basis points, resulting in 12.3% organic revenue growth, exceeding our guidance range of approximately 11%. Full year 2023 adjusted earnings per share of $2.05, grew 20% versus 2022, exceeding the high end of our guidance range of $1.99 to $2.02. Adjusted gross margin for the fourth quarter was 70.4%, resulting in full year 2023 adjusted gross margin of 70.7%, in line with our expectations and representing a 20 basis point improvement versus full year 2022, inclusive of a 220 basis point headwind from foreign exchange. In 2024, we expect a mixed benefit from our new launches with offsetting headwinds from FX and the incremental investment in our manufacturing capacity.

And as a result, we anticipate our full year 2024 adjusted gross margin will be at or slightly below our full-year 2023 rate. Fourth quarter adjusted operating margin was 26.6%, resulting in a full year 2023 adjusted operating margin of 26.3%, improving 70 basis points versus 2022. We expect to expand adjusted operating margin in 2024 by another 30 basis points to 50 basis points, balancing progress towards our long-range plan goal of 150 basis points over the three years, 2024 to 2026, with flexibility for critical investments to support key launches. On a GAAP basis, the fourth quarter operating margin was 15.7%, resulting in a full year reported operating margin of 16.5%. Moving to below the line, fourth quarter adjusted interest and other expenses totaled $79 million, resulting in full year adjusted interest and other expenses of $331 million in line with our expectations.

On an adjusted basis, our tax rate for the fourth quarter was 10% and 11.2% for the full year 2023, including favorable discrete tax items and the benefit from stock compensation accounting. Our operational tax rate was 14.6% for the fourth quarter and 13.9% for the full year, again in line with expectations. Fully diluted weighted average shares outstanding ended at 1,477 million shares in Q4 and 1,464 million shares for full year 2023. Free cash flow for the quarter was $718 million with $984 million of operating activities, less $267 million of net capital expenditures. Excluding special items, adjusted free cash flow was $913 million. Full year 2023 cash flow was $1.8 billion and adjusted free cash flow was $2.5 billion, both in line with expectations.

For 2024, we expect full year free cash flow to be in excess of $2 billion, which includes approximately $800 million of expected payments related to acquisitions, restructuring, litigation and other special items. As of December 31st, 2023, we had cash on hand, $865 million, and our gross debt leverage was 2.3 times. We expect to fund the Axonics acquisition through a mix of cash on hand and new debt, which will be determined prior to or at the time of close. Our top capital allocation priority remains strategic tuck-in M&A, followed by annual share repurchases to offset dilution from employee stock grants. Our legal reserve was $377 million as of December 31st, a decrease of $30 million versus the prior quarter, $108 million of this reserve is already funded through our qualified settlement funds.

Now I’ll walk through guidance for the first quarter and the full year 2024. We expect full year 2024 reported revenue growth to be in a range of 8.5% to 9.5% versus 2023. Excluding an approximate 50 basis point headwind from foreign exchange based on current rates, we expect full year 2024 operational revenue growth to be 9% to 10%, excluding a 100 basis point contribution from closed acquisitions, we expect full year 2024 organic revenue growth to be in a range of 8% to 9% versus 2023. We expect first quarter 2024 reported revenue growth to be in a range of 7.5% to 9.5% versus first quarter 2023. Excluding an approximate 100 basis point headwind from foreign exchange based on current rates, we expect first quarter 2024 operational growth to be 8.5% to 10.5%, excluding a 150 basis point contribution from closed acquisitions, we expect first quarter 2024 organic revenue growth to be in a range of 7% to 9% versus Q1 2023.

We expect our full year 2024 adjusted below the line expenses to be approximately $330 million. Under current legislation, including enacted laws and issued guidance under OECD Pillar Two rules, we forecast a full year 2024 operational tax rate of approximately 14% and an adjusted tax rate of approximately 13%. We continue to monitor tax legislation globally, including the currently drafted law to partially repeal US R&D capitalization. If the law were to be passed as currently proposed, we would expect a tailwind of approximately 100 basis points to our operational tax rate in 2024. We expect full year adjusted earnings per share to be in a range of $2.23 to $2.27, representing 9% to 11% growth versus 2023, including an approximate $0.04 headwind from foreign exchange at current rates and existing hedging contracts, which will be recognized ratably through the year.

We expect first quarter adjusted earnings per share to be in a range of $0.50 to $0.52. For more information, please check our investor relations website for Q4 2023 financial and operational highlights, which outlines more details on Q4 and full year results and 2024 guidance. In closing, I’m very proud of our 2023 performance and look forward to executing on our 2024 guidance of 8% to 9% organic revenue growth, 30 basis points to 50 basis points of adjusted operating margin expansion and adjusted EPS growth of 9% to 11%. Before I turn it back over to Lauren for the Q&A, I wanted to provide a quick update. A key part of our talent strategy is moving high-potential individuals throughout the company to give them a broad set of experiences. As part of this, effective March 1st, Lauren Tengler will become the Global Controller for our Urology business unit, providing financial leadership to the global business and importantly, playing a key role in the integration of the Axonics business.

Lauren previously spent many years within our Urology business, making her uniquely qualified for this opportunity. Following Lauren’s transition, Jon Monson, currently our Chief Accounting Officer, will move to our Investor Relations function, leading Ally DeVoe and the rest of the team. I know the investment community will join me in thanking Lauren for her leadership and contributions and in welcoming Jon to the role. With that, I’ll turn it back to Lauren, who will moderate the Q&A.

Lauren Tengler: Thanks so much, Dan. Drew, let’s open it up to questions for the next 30 minutes or so. In order for us to take as many questions as possible, please limit yourself to one question. Drew, please go ahead.

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Q&A Session

Operator: Thank you. We will now begin the question-and-answer session. [Operator Instructions] The first question comes from Robbie Marcus with JPMorgan. Please go ahead.

Robert Marcus: Oh, great. Congrats on a really good quarter and congratulations, Lauren, on the promotion. Wanted to ask on two of the biggest product drivers in 2024, WATCHMAN and FARAPULSE. FARAPULSE got approval today. Wanted to see what’s included in guidance for this year and how to think about phasing over the year. How long will it take to get into hospitals and approved on formularies? And then second on WATCHMAN, look, still had a very good quarter and fourth quarter, but growth slowed a little bit. How should we be thinking about the potential for WATCHMAN and 20% plus growth in 2024? Thanks a lot.

Michael Mahoney: Sure. Thanks, Robbie, for the comments. I’ll start with the WATCHMAN, just an excellent platform with the growth of 23% for the quarter, 25% for the full year. Terrific work. And as you know, that product gets larger and larger for us. I had to cut the script back because the clinical investments we’re making with WATCHMAN will go on for a while, and we can touch on those if interested. But as you know, we continue to exceed likely 90% share in the US. We’ll be rolling out WATCHMAN Flex Pro, you know, more as a percent of our total mix in the US in the first quarter and throughout the year. So you’ll continue to see that, which is a differentiated platform. So with the clinical work that we’re doing and the WATCHMAN Flex Pro and the Steerable Sheath likely to be in the market in 2024 as well, we continue to expect to gain share, and we aim to significantly widen the market opportunity through these clinical trials.

So full steam ahead with WATCHMAN. On FARAPULSE, maybe the most exciting day I’ve had in my career at Boston Scientific with this platform that we have, based on the results that we’ve seen in Europe and the enthusiasm globally for our PFA platform. And to receive approval today was really exciting. We did anticipate a first-quarter approval for FARAPULSE. And as you might expect, we expect the impact of FARAPULSE to be, you know, somewhat in the first quarter and much more significant as the year goes on as we work with contracting with hospitals, getting on contract and getting the capital approved and rolling it out. But we have a lot of experience in doing that through our European success that we’ve enjoyed. Our team is trained. We have installation team.

We continue to invest in it. So we’re really excited about aiming to disrupt the EP market with what we think is the premier PFA platform.

Robert Marcus: Great. Thanks a lot.

Operator: The next question comes from Joanne Wuensch with Citi. Please go ahead.

Joanne Wuensch: Thank you and good morning. I don’t want to leave FARAPULSE quite yet, and I suspect there’ll be a lot of questions on it this call. But if you’re looking for China and Japan approval in the second half of ’24, could you sort of outline what you think those opportunities maybe? And then can you just give a quick highlight on some of the other sort of higher profile cardiology companies such as POLARx and AGENT? Thank you.

Michael Mahoney: Yeah, so Ken can help me out. But obviously China and Japan represent significant opportunities in the EP market. They’re the largest markets that we compete in — in those countries and we currently are under-scaled, particularly in China. In Japan, we built a lot of momentum over the last, call it, 18 months with our POLARx launch. So in Japan, you know, that grew, I don’t know, I think over 40%, our EP business. And so we have a more scaled commercial team capabilities in Japan. And the eventual approval in the second half of this year in Japan with FARAPULSE will really be, you know, the next leg of the growth stool in Japan for us. So a lot of confidence there. The market in China may be even bigger. We’re a bit more under-scaled in China, so we’ll be making a lot of investments there.

We have a brand new leader. We’re excited about in China to run our EP business under June Chang. So we’ll be making additional commercial investments, clinical investments, and hope to have approval in the second half of the year in China. So those will be nice growth drivers for us in ’24, more significant in 2025. And AGENT, Ken, do you want to comment a bit more on FARAPULSE? Dr. Stein?

Kenneth Stein: I mean, I love to comment on FARAPULSE. Again it is a very exciting day. Joanne, in terms of the questions specifically about Japan and China, right. I think we got to realize I mean, AFib is a global disease. I hate to use the word pandemic, but it is pandemic. Now and we’re really pleased about the strength of the clinical trial data that we have as well as the commercial experience in Europe with, as Mike said, you know, greater than 40,000 patients already treated to-date. And it’s that strength of the clinical data, right, that led us to the really, I think, rapid approval that we got from the FDA, and that has led us to update our anticipated approval times both in Japan and China. Again, I think having said that, you know, we look to those approvals in the second half.

So I don’t think we’re going to expect to really see too much material out of that until we get into 2025. But they are both large and important markets and large and important patient populations that are currently really very much underserved in terms of access to Ablation technology.

Joanne Wuensch: AGENT.

Michael Mahoney: Thanks, Joanne

Operator: Thank you. The next question comes from Larry Biegelsen with Wells Fargo. Please go ahead.

Larry Biegelsen: Good morning. Thanks for taking the questions. Congrats on a strong finish here and the approval of FARAPULSE in the US. On FARAPULSE, can you talk about the manufacturing capacity for the catheter and console upon launch? And expectations for the EP business this year? You know you grew 43% in Q4’23. Any reason why growth would be lower in ’24? And I have to ask you to please clarify your comments around ACURATE Neo2. It sounds like something happened with Prime, which is the larger size. What are the implications for the other sizes of Neo2 in Europe and the US? Thank you.

Michael Mahoney: Thanks, Larry. Starting with FARAPULSE, really very proud of the global supply chain team and what they’ve done over the past 18 months in the FARAPULSE Group that we originally acquired a while ago. But they’ve done a tremendous job in building capabilities to supply this for the US launch and to expand in Europe, and eventually Asia, as we just highlighted. So we are now significantly improved our catheter and console supply. We opened numerous centers in Europe in the fourth quarter and we’re ready to go. So we, at this point, don’t anticipate supply being an issue to continue to support Europe or to facilitate the US launch, given the capabilities and investments that we’ve made in approvals to manufacture in multiple locations.

So great work by the supply chain team. And we’re ready to launch this in the US. On ACURATE Neo2, as I mentioned in the earnings script, maybe just two overall points. We continue to do very well with ACURATE Neo2 in Europe, implanting, I think, the number 70,000, and continuing to grow faster than the market in Europe. And we are on track for what we have is called Prime in Europe in 2025. So that continues to move forward as planned. With respect to the trial, as I mentioned in the script, based on the interim analysis, we now need to wait for the full one year follow up of the 1,500 patients. And as a result of that, we don’t — we will not be receiving approval for ACURATE Neo2 in 2024. And we will wait until likely near the end of 2024 for the full readout of the ACURATE IDE study to determine our path forward.

Larry Biegelsen: Thank you, and congrats, Lauren.

Lauren Tengler: Thanks, Larry.

Operator: The next question comes from Vijay Kumar with Evercore ISI. Please go ahead.

Vijay Kumar: Hey, guys. Thanks for taking my question and congrats on a really strong finish here. Maybe just one on the guidance here perhaps for Dan. Dan, the 8% to 9%, it looks like FARAPULSE, the prior guided, I’d assume, a back half launch. It’s coming in a little bit ahead. Can you just, you know, walk us through the 8% to 9%. Is that right that FARAPULSE, perhaps, assumptions have changed? Any impact from VBP or base impact that we should be aware of? And what is — what are you assuming for pricing in fiscal ’24? Thank you.

Daniel Brennan: Sure. So the VBP assumptions are the same as they’ve always been, really no change there. As you saw, in December, when we issued the press release on AVANT GUARD, we moved up the timing of expected FARAPULSE launch to Q1. So we’ve been anticipating Q1 launch. And that 8% to 9% full year and the 7% to 9% for the first quarter in terms of revenue growth contemplated a Q1 approval of FARAPULSE, as Mike said, you know, there’s probably some contribution in Q1, but more of that contribution comes in Q2 to Q4. So the 8% to 9% has that contemplated in the overall guide. And then pricing, so I would say on pricing is, we were basically flat in 2023 and the goal is to be flat again in 2024. So likely no impact would be the goal in 2024 versus 2023.

Vijay Kumar: Fantastic. Sorry, on days, Dan? Any days impact here?

Daniel Brennan: No, all the days — there’s a lot of, obviously, a lot of noise in days around the world through the year. It’s all contemplated in the guidance. All in the 8% to 8% for the full year.

Vijay Kumar: Fantastic. Thank you guys.

Michael Mahoney: Sure, Vijay. Thanks.

Operator: The next question comes from Danielle Antalffy with UBS. Please go ahead.

Danielle Antalffy: Hey, good morning, everyone. Thanks so much for taking the question. Just a follow-up question on ACURATE Neo2, Mike, if I could. So appreciate the comments that you did provide. Just curious, I mean, obviously, you’re giving pretty strong guidance here for 2024. I mean, is the right read here that regardless of what happens with ACURATE Neo2 and timing there, you’re sticking to your long-term sales growth guidance that you provided back in September. And sort of how do we think about this as a long-term growth contributor now, given this little wrinkle here? And Lauren, we will miss you very much. Thanks so much.

Michael Mahoney: Lauren is not leaving the company. She will be around. She’ll be around. We’re still going to see her.

Danielle Antalffy: But we won’t get to see her, so.

Michael Mahoney: Okay, well.

Danielle Antalffy: I’ll work my way in.

Michael Mahoney: We’ll work our way in, right, once in a while. So we’re excited for John to come in and Lauren to move out. No, excited for Lauren to go to Urology. Yes. So to answer your question, we are fully committed to the 8% to 10% organic growth CAGR over the ’24 to ’26 period that we provided in Investor Day. Absolutely no change in that outlook. And pleased with the ’23 performance, as you know, where we grew 12%. So absolutely no change to those financial goals. You know, ACURATE continues to do well in Europe. It’s a product that’s used every day by many European physicians and we’re excited about getting the larger size approved there. We are disappointed that we didn’t get ACURATE over the goal line for approval in 2024.

So at this point, we need to wait until the full data sets been followed up for a year and read out likely before the end of this year in 2024. And we’ll take it from there in terms of the US launch. But we are disappointed we’re not going to launch that really very end of this year and into next, but absolutely no change to our financial guidance that we gave at Investor Day.

Danielle Antalffy: Okay. Great. And also welcome, Jon. Sorry, I didn’t mean to leave you out. Thanks so much guys.

Jon Monson: Thanks, Danielle.

Operator: The next question comes from Travis Steed with Bank of America. Please go ahead.

Travis Steed: Hey, thanks for taking the question. Maybe one more follow-up on TAVR. Can you just remind us what the interim look was? Was that just like a six-month look at the data? Now you need to wait for one-year data for the line to separate. And curious if you think what you saw in the interim look. Are you still pretty confident that at one year? We could have a US TAVR launch? Or does this put the whole US TAVR launch at risk?

Michael Mahoney: Janar, Are you able to hear us okay?

Janarthanan Sathananthan: Yes, I can hear you loud and clear.

Michael Mahoney: Great. Dr. Sathananthan is our Chief Medical Officer, as you know, for ICT and Structural Heart. Maybe he could comment a bit.

Janarthanan Sathananthan: Yeah. I’ll take the comment just about the data. So essentially what happened in the trial was that as part of a planned interim analysis, we made the decision to await the full one-year data. It is important just to note that the accurate IDE study is still an active clinical study with active clinical follow-up. And so as a result, we cannot disclose any data related to the trial at this time. We will expect, as Mike said, a readout of the study in the second half of 2024, following a full data review.

Travis Steed: Great. Thank you.

Operator: The next question comes from Josh Jennings with TD Cowen. Please go ahead.

Josh Jennings: Good morning. Thanks for taking the questions and congratulations for a strong end of the year. Wanted to ask about the international cardiac ablation market. Boston, incredible fourth quarter, 40% plus growth. Some of your competitors delivered really strong international growth in their electrophysiology businesses as well. What’s going on in the international market? I mean, are we seeing the promise of PFA driving market expansion this early? Or is there any pricing dynamics going on? But I think it’s 20% almost market growth in internationally for cardiac ablation this year. Just wanted to get some details there and whether that could translate to PFA launches in the United States, driving market expansion, which I think you guys detailed in your Investor Day. Thanks for taking the question.

Michael Mahoney: Dr. Stein, do you want to take a shot on it?

Kenneth Stein: Yes, Josh, and thanks, Mike. I think it’s a couple of factors here, and I don’t know that I can parse out for you, you know, how much is getting contributed from each. But again, I think we just begin with the fact, right, that atrial fibrillation is an incredibly common arrhythmia. Again, as I said earlier, it is literally pandemic worldwide. I know, for instance, in the US, right, a quarter of adults over the age of 40 will experience Afib at some point in our lives. And ablation, even with legacy thermal technologies, things for us, like stable point or POLARx is incredibly effective. It’s more effective than drugs. But on a global scale, it is still really incredibly underpenetrated as a market. And much of the growth that you see, really just reflects, I think, you know, increasing realization in the cardiology community, the referring physician community, about the relative efficacy and safety of all ablation technologies.

And then you layer on top of that the promise and the data of FARAPULSE, right? And FARAPULSE, again, it takes a procedure that’s already effective. It is at least as effective. It is clearly safer. And it’s also much more efficient than thermal ablation. And so that, right, enables docs and medical centers to scale this out much better, right, and start to get into this underpenetratrated population. So maybe a long-winded answer, but the short answer is, right, it’s both a dramatically underpenetrated population to begin with, and then on top of that, you have the accelerated impact of FARAPULSE.

Josh Jennings: Appreciate it. Thank you.

Operator: The next question comes from Richard Newitter with Truist Securities. Please go ahead.

Richard Newitter: Hi. Thanks for taking the questions and congrats on a really strong finish to the year.

Michael Mahoney: Thanks.

Richard Newitter: My first question is just going back to TAVR. You know, at your Analyst Day, you had talked to, you know, an expectation and a level of confidence that you could disrupt that market in the US relatively quickly out of the gate. I’m just curious with, you know, and get something approaching 20% share of the market over time, which is what you’ve done, you know, in other markets with your disruption capabilities. I’m just curious, does anything change there with the indeterminate kind of view of what the next steps are for the US? I’m just trying to focus on that commentary a bit. You know, does your outlook for the franchise in the US change in TAVR? And then I have a follow-up.

Kenneth Stein: Yeah. Just a few clarifying points. Again, in Europe, where we set 70,000 valves and physicians use it routinely on an everyday basis. We continue to grow faster than the market there and have continued to done that for, I don’t know, 10 quarters in a row. So we make nice progress. And we’re excited about getting the large valve size approved in Europe. I believe in 2025 is the time period. In the US, you know, honestly, first of all, I would state that we’ve never quoted a market share goal for TAVR in the US. So we never said 20. I’m not sure if that was what you put in your models or not. But based on the results that we’ve seen in Europe, we’ve always been confident in our ability to have ACURATE be a meaningful growth driver in the US, as we stated in Investor Day.

You know, as a result of this, we are disappointed that, you know, we’re not going to have this launched in 2024. As we talked about, based on the data that we just highlighted in the script, and as Janar mentioned, we now need to wait for the full year data, the full one-year follow-up on the 1,500 patients, and then working with the FDA and submitting that and having a data readout by year-end 2024. And we’ll take it from there. So we — as Janar said, the trial is still active. So we do not expect any of this news to alter our 8% to 10% organic growth over the three-year period. We’re coming off of 12%. We continue to grow faster than most all of our peers and drop EPS faster than our peer group. And we’re still very committed to those financial targets.

And we’re hopeful that ACURATE will continue to be a big growth driver for us. But a lot of it depends on that data readout in fourth quarter ’24.

Richard Newitter: Okay. Thanks for that. And then maybe just on M&A, you know, you’ve been active in 2023 and congrats on Relievant and more recently Axonics early this year. I’m just curious on kind of how we should think about, you know, how aggressive and opportunistic you’ll be over the next twelve months. You mentioned, obviously your first priority remains deploying capital for tuck-ins. You know, but do we kind of think of you guys in a little bit of a digestion period or kind of steady she goes just as aggressive and opportunistic as you have been in the past?

Daniel Brennan: Sure, I can take that one. So as you mentioned, Axonics, the most recent deal we did. Super pleased with that. I think that is a classic tuck-in for Boston Scientific. It’s one, I think, we — as you look back, these types of deals, we really do well with and we’re super excited to have that close and welcome the Axonics team into the BSE family. As you said, we’ve been remarkably consistent over a long period of time. Tuck-in M&A is still the number one capital allocation priority for us and will continue to be active. In terms of how active over the near-to medium-term. This is not a major event like a major delevering event that we need to do. This is — take on a little bit of additional debt over a period of time. And then over a very reasonable period of time, we’ll be right back to where we are today relative to our leverage goal. So I look us — I look for us to continue to be active in the tuck-in M&A space in ’24 and beyond.

Richard Newitter: Okay. Again, congrats on an outstanding 4Q.

Michael Mahoney: Thank you.

Daniel Brennan: Thank you.

Operator: The next question comes from Patrick Wood with Morgan Stanley. Please go ahead.

Patrick Wood: Amazing. Thank you for taking the question and congrats, Lauren. I’d like to stick with Axonics, if that’s all right. I appreciate it hasn’t closed yet. But I’m just kind of curious, you know, Urology in Boston has a very sizable distribution network across, I guess, primarily Stone Management, but a whole bunch of different areas. How are you thinking about, you know, the ability to drive adoption in OAB faster and like really push that asset? I’m guessing, you know, having just played with the numbers, and correct me if I’m wrong, but there’s some assumption of slightly faster growth once you’ve acquired Axonics and the Street previously had in there. At least that’s where I end up with the numbers. Feel free to correct me. But how are you thinking about the commercialization really pushing that through the distribution network? Thanks.

Michael Mahoney: Sure. Well, we haven’t closed it yet. We hope to first half this year. You know, the team at Axonics done an amazing job with this platform since starting the company years ago and taking significant share and what is a strong double-digit growth market. The team at Axonics, you know, can’t speak too much for them. It hasn’t closed yet, has also done a remarkable job in a few areas. One at just the core technology where they gain — leveraged that to gain share, the clinical data that they have, the commercial excellence that they possess, and also expanding the market through their direct-to-patient marketing and awareness. So this is a significant global opportunity. And the patient awareness of this treatment is still early days.

And so that’s one reason why we acquired the company was the momentum they have the technology and the long-term market cater that we see based on the global opportunity. The market today is reasonable nearly all US. That’s something we’ll evaluate more in the future here as to would it make sense for us to bring this to select markets outside the US, given the data that we have? As you mentioned, we have a significant commercial channel in our Urology business through all of our different business units within Urology. So this is an ideal fit. It is an adjacency for us. We don’t have any competitive product in this area. So it’s a nice adjacency for us that will allow us to compete more comprehensively with Urology customers. But we aim to, you know, take Axonics to the next level, but that team has done a terrific job to date.

Patrick Wood: Amazing. Thanks for taking the question.

Michael Mahoney: Sure.

Operator: And just to verify, do we have time for one more question?

Lauren Tengler: Yes. One last question, please.

Operator: Okay. That question will come from Michael Polark with Wolfe Research. Please go ahead.

Michael Polark: Good morning. Thanks for sneaking me in. I’ll ask a gross margin question. Dan, I heard in the script for ’24 flat to maybe slightly down year-on-year in the guide. The world seems to be calmer on price cost, but as we all know, the Middle East is flaring. And so, I’m curious, one, have you built in any cushion for kind of cost-push from those events? And two, in real-time, are you seeing any impact in the field? And if so, what does that look like?

Daniel Brennan: Yeah, I can give you the short answer and a little bit longer answer. So the short one is that we’ve contemplated all that. Our team is super close to everything relative to our global supply chain network. And so there — everything that we have in the guidance that we gave contemplates what we know today and what — and the guidance that they’re giving us on that, which — the impact is minimal. Overall on gross margin, the little bit longer answer. You know, if you look at ’23, we came in pretty much right where we expected at that 70.7%. And then, as we said at the Investor Day in September, we said it would be a challenge to contribute to our margin expansion goals in ’24, right, which that’s probably going to prove out to be true because we’re saying we’ll be either at or slightly below.

But that’s okay, as there are many other areas of the P&L, and as you know, we have a pretty solid track record over time of managing all those lines of the P&L to drive margin expansion, most recently that 70 basis points last year. So for ’24, I’d kind of point to two headwinds and two tailwinds that will play out, and, again, have us at that kind of at or slightly below the 70.7% we put up last year. And one is inflation. And that’s probably a little bit of a tailwind, right? So the macro factors are improving, in general, relative to inflation and other things. But as a reminder, we entered into, you know, contracts for many elements of materials for 2024 already last year. So we don’t see that full benefit. But in ’25 and ’26, I’d like to believe there’s even more benefit there, not only from the macro side of inflation, but also for gross margin in total.

And then our mix, so you know, getting the FARAPULSE approval today, that’s exciting because that’s a great mix thing for the company, and many of our other launches are as well. And then on the headwind side, foreign exchange was a headwind in ’23, that continue in ’24. And as I said, at Investor Day, good problem to have, but we also need to make investments in manufacturing capacity to support the sales growth, you know, growing 12% last year and then 8% to 9% this year. But we’re absolutely committed to the 150 basis points over three years. Gross margin probably won’t pay a lot of bills for us in ’24, but I think it certainly will in ’25 and ’26. Recall, we used to be north of 72% back in 2019. And we are maniacally focused to get there and then to get the overall operating margin kind of, you know, on the doorstep of 28 when we get to 2026.

And that puts that 30% long-term goal that we’ve had kind of right in our line of sight as we’re in 2026.

Michael Polark: Thank you.

Michael Mahoney: Thank you.

Lauren Tengler: Thanks for joining us today. We appreciate your interest in Boston Scientific. If we were unable to get to your question or if you have any follow-ups, please don’t hesitate to reach out to the Investor Relations team. Before you disconnect, Drew will give you all of the pertinent details for the replay.

Operator: Thank you. Please note, a recording will be available in one hour by dialing either 1-877-344-7529 or 1-412-317-0088 using replay code 2394361 until February 7th, 2024, at 11:59 PM Eastern Time. The conference has now concluded. Thank you for attending today’s presentation. You may now disconnect.