Earnings release
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NEWS RELEASE Edwards Lifesciences Reports Third Quarter Results 2026-11-04 IRVINE, Calif.--(BUSINESS WIRE)-- Edwards Lifesciences (NYSE: EW) today reported nancial results for the quarter ended September 30, 2026. Q3 Financial Highlights Q3 sales grew 10.5% to $1.72 billion 1, constant currency 2 sales grew 11.2% Q3 TAVR sales grew 8.0% to $1.24 billion 1, constant currency 2 sales grew 8.8% Q3 TMTT sales grew 44.0% to $207 million 1,3, constant currency 2 sales grew 45.6% 3 Q3 EPS of $0.53 1; adjusted 2 EPS of $0.80 1 which grew 19% versus prior year 2026 Outlook Increasing total company sales 2 growth guidance to approximately 11.5% from 10% to 11% Increasing TAVR sales 2 growth guidance to 9.0% to 9.5% from 8% to 9% Increasing TMTT sales guidance to $780 to $790 million from $760 to $780 million Increasing adjusted EPS guidance to $2.97 to $3.05 from $2.95 to $3.05, growing 18% at midpoint versus prior 1
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year 2026 performance and milestone achievements reinforce long-term durable growth Recent Highlights PROGRESS trial marks turning point in the management of moderate AS Practice-changing data adding to Edwards’ body of structural heart clinical evidence presented at TCT Final TAVR NCD represents important step toward expanding access to timely, high-quality care U.S. approval of PASCAL Precision for tricuspid repair expands access to di erentiated therapy U.S. approval of PASCAL Ace with Capture Clarity simpli es mitral device placement European approval of SAPIEN M3 RESILIA brings most advanced tissue treatment to patients U.S. approval of AUTUS addresses lifelong needs of pediatric patients with congenital heart disease “We delivered strong third-quarter growth of 11.2% which exceeded expectations, with broad-based performance across our businesses and regions, giving us the con dence to raise our full-year outlook,” said Bernard Zovighian, CEO of Edwards Lifesciences. “Our focused structural heart strategy, coupled with disciplined execution, long-term investments in category-creating innovation, and commitment to science and technology advancements, enabled us to deliver signi cant progress for patients on several of our most important clinical, regulatory, policy and commercial priorities this quarter. As I re ect on 2026 so far, I am proud of what our teams have accomplished and how we are positioning Edwards for strong, sustainable growth over the long term.” Transcatheter Aortic Valve Replacement (TAVR) In the third quarter, the company reported TAVR sales of $1.2 billion, which increased 8.0% compared to the prior year, or 8.8% on a constant currency basis. Edwards’ growth rates were similar in the U.S. and outside of the U.S. Globally, procedural growth bene ted from a heightened focus on TAVR and data supporting proactive disease management of severe aortic stenosis (AS). Exiting Q3, the company saw encouraging signs of procedure growth. After several quarters of modest share gains, Edwards is pleased with how its competitive position, supported by its di erentiated SAPIEN platform, has contributed to year-to-date TAVR performance. Average selling prices were stable globally. In the U.S., procedure growth continued to bene t from a heightened focus on TAVR therapy as the clinical community further incorporates into practice the meaningful evidence supporting proactive disease management. Edwards’ competitive position in the U.S. was stable sequentially and increased modestly year-over-year, enabled by strong adoption of its SAPIEN 3 Ultra RESILIA platform. During the quarter, the Centers for Medicare & Medicaid Services (CMS) released the nal, updated national coverage determination (NCD) for TAVR. The updated policy represents an important step toward improving and expanding timely, high-quality access to care while reinforcing 2
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the value of the multidisciplinary heart team. Outside of the U.S., the company continues to see strong adoption of its SAPIEN technology. In Europe, updated ESC and EACTS guidelines are helping shape clinical discussions around earlier intervention and proactive disease management, further reinforcing the role of TAVR across a broader patient population. In Japan, Edwards was encouraged by the growth and continued adoption of its SAPIEN 3 Ultra RESILIA platform. Also in Japan, Edwards secured new and dedicated reimbursement for the SAPIEN 3 Ultra RESILIA platform, which recognizes the value of its innovation and helped contribute to Japan’s strong performance in the quarter. Transcatheter Mitral and Tricuspid Therapies (TMTT) Third quarter TMTT sales of $207 million3 increased 44.0% compared to the prior year, or 45.6% on a constant currency basis. Results were driven by the company’s di erentiated portfolio of repair and replacement therapies. Globally, mitral and tricuspid procedure volumes continued to grow in the double digits. The value of the company’s TMTT portfolio is evident as its mitral and tricuspid therapies advance along their adoption curves, allowing physicians to personalize care for each patient’s unique needs. Adoption of Edwards’ PASCAL system continues to strengthen, supported by the di erentiated design and clinical outcomes of the platform and the company’s portfolio approach. During the quarter, the PASCAL ACE with Capture Clarity implant received U.S. approval for use in degenerative mitral TEER procedures and a measured rollout of the technology is underway. The PASCAL Ace with Capture Clarity implant is the rst FDA-approved TEER device to include novel indicators that provide con rmation of the challenging step of lea et grasping. In October, the FDA approved the PASCAL Precision system for tricuspid regurgitation, expanding access to this important therapy for patients. Early clinician feedback is very positive on both the PASCAL Ace with Capture Clarity implant and the PASCAL system for tricuspid. Clinicians value the simpli cation of device placement with the new features of the Capture Clarity technology. With the PASCAL tricuspid system, physicians are recognizing that unique features, including device elongation, are particularly bene cial for patients with complex tricuspid anatomy. The company’s focus on continued innovation with the PASCAL system represents a positive step forward for patients in need of mitral and tricuspid repair. The EVOQUE system delivered another strong quarter of growth. As physicians gain experience with the therapy, they are more consistently achieving mild or less residual regurgitation, a result that is increasingly linked to better outcomes for patients. The company also recently received U.S. and European approval for the EVOQUE system for transjugular access, enabling patients with complex femoral access to bene t from the procedure. The company continues to see strong demand for the SAPIEN M3 system for patients who are not suitable for 3
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mitral TEER, supported by excellent early clinical outcomes. In addition, Edwards introduced the SAPIEN M3 system with RESILIA tissue in Europe this quarter. Surgical In Surgical, third quarter global sales of $264 million increased 2.5% compared to the prior year, or 2.8% on a constant currency basis, driven by continued adoption of the company’s RESILIA tissue portfolio of surgical therapies. Edwards continues to expand its Surgical portfolio with innovative technologies that address additional unmet patient needs in structural heart surgery. During the quarter, AUTUS became the rst FDA-approved surgical pulmonary valve designed speci cally for pediatric anatomy with the ability to expand as a child grows, potentially reducing the need for repeat open-heart surgeries. The company is also advancing a measured rollout of ECLIPTIS, its surgical left atrial appendage system in the U.S., prioritizing exceptional outcomes for patients through physician training and procedural excellence. TCT 2026 Highlights At TCT 2026, physicians presented compelling new evidence on the SAPIEN, PASCAL, EVOQUE and SAPIEN M3 systems that deepen the clinical community’s understanding of these therapies and underscore their signi cant potential to transform care for AS, mitral and tricuspid patients. The breadth and quality of this evidence re ects the strength of Edwards’ innovation strategy and its commitment to setting the benchmark for clinical evidence in structural heart disease. In TAVR, results from the PROGRESS trial were presented and simultaneously published in The New England Journal of Medicine, marking a turning point in the management of moderate AS. Additionally, new long-term economic data from the EARLY TAVR trial reinforced the value of proactive disease management. In patients with asymptomatic severe aortic stenosis, Edwards TAVR delivered strong economic value compared with clinical surveillance and remained highly cost-e ective even after accounting for potential future valve reintervention. In TMTT, multiple important studies on Edwards’ portfolio of mitral and tricuspid repair and replacement therapies were also shared. The CLASP IITR pivotal trial demonstrated superiority of the PASCAL system plus optimal medical therapy (OMT) compared with OMT alone in patients with severe or greater tricuspid regurgitation. This was driven by signi cant improvements in health status for those receiving the PASCAL device. In addition, results from 1,100 EVOQUE TTVR patients in the TVT Registry with CMS linkage demonstrated that real-world clinical outcomes of patients with more complex disease replicate those observed in the TRISCEND II clinical trial. Finally, the ENCIRCLE 4
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trial studying two-year outcomes of the SAPIEN M3 system, supported transseptal TMVR as a therapeutic option for selected patients with mitral regurgitation. Additional Financial Results For the quarter, gross pro t margin was 78.5%, or 78.7% adjusted compared to 77.9% in the same period last year. Expected impact from the scaling of newer therapies was more than o set by manufacturing e ciencies and foreign exchange. The company continues to expect adjusted gross pro t margin to be at the lower end of its full- year 78% to 79% gross margin guidance, driven by the impacts of currency uctuations through the company’s hedging program. Selling, general and administrative expenses in the third quarter were $561 million, or 32.7% of sales, compared to 33.1% of sales in the prior year. This was in line with the company’s expectations and re ects continued investment in resources to support patient access and care. Research and Development (R&D) expenses in the third quarter were $281 million, or 16.4% of sales, compared to 18.1% in the prior year. These investments in innovation re ect Edwards’ focus on expanding its structural heart portfolio. The company expects R&D expense as a percentage of sales to be approximately 16.5% in 2026. Operating pro t margin in the third quarter was 17.4%, or 30.3% adjusted. Adjusted EPS of $0.80 bene ted from better-than-expected topline performance as well as planned phasing of strategic investments in R&D and SG&A throughout the year. In 2026, Edwards continues to expect full-year operating pro t margin to be at the high end of the company’s original 28% to 29% guidance range, resulting in approximately 150 basis points of constant currency operating margin expansion for the full year. Edwards continues to expect its 2026 e ective tax rate, excluding special items, to be at the high end of its previous range of 16% to 19%. This re ects an expectation that side-by-side safe-harbor taxation legislation related to Pillar Two does not come into e ect before the end of the year. The company’s tax rate is also impacted by changes to California law restricting the usage of R&D credits. Cash and cash equivalents were approximately $3.1 billion as of September 30, 2026. Total debt was approximately $600 million. Edwards has performed share repurchases of approximately $700 million through the third quarter and has approximately $1.3 billion remaining under its share repurchase authorization. Outlook 5
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As a result of the company’s strong third quarter results, Edwards is increasing its full-year 2026 sales growth rate guidance to approximately 11.5% from 10% to 11% and TAVR product group sales growth guidance to 9% to 9.5% from 8% to 9%. In the fourth quarter and going forward, Edwards assumes that growth will be mainly driven by continued increases in procedure volumes and less by share gains. The underlying market dynamics in TAVR are strong and we saw positive procedure growth trends exiting the quarter. In addition, Edwards is increasing TMTT product group sales guidance to $780 to $790 million from $760 to $780 million and is increasing adjusted EPS guidance to $2.97 to $3.05 from $2.95 to $3.05. The company is also rea rming mid-single-digit growth guidance in Surgical. For the fourth quarter of 2026, the company projects total sales to be between $1.67 and $1.75 billion and adjusted EPS of $0.61 to $0.69. About Edwards Lifesciences Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world-class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient-focused culture to deliver life-changing innovations to those who need them most. Discover more at www.edwards.com and follow us on LinkedIn, Facebook, Instagram and YouTube. Conference Call and Webcast Information The company will be hosting a conference call today at 2:00 p.m. PT to discuss its third quarter results. To participate in the conference call, dial (877) 704-2848 or (201) 389-0893. The call will also be available live and archived on the “Investor Relations” section of the Edwards website at ir.edwards.com or www.edwards.com. This news release includes forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, and Section 21E of the Securities Exchange Act of 1934. These forward-looking statements can sometimes be identi ed by the use of words such as “may,” “will,” “should,” “anticipate,” “believe,” “plan,” “project,” “estimate,” “forecast,” “potential,” “predict,” “early clinician feedback,” “expect,” “intend,” “guidance,” “outlook,” “optimistic,” “aspire,” “con dent” or other forms of these words or similar expressions and include, but are not limited to, statements made by Mr. Zovighian; statements in the 2026 Outlook section and recent highlights section; statements in the Additional Financial Results and Outlook sections; statements regarding how we are positioning Edwards for strong, sustainable growth over the long term, encouraging signs of procedure growth; competitive position remaining steady heading into next year; adoption of our technologies in various regions; AUTUS potentially reducing the need for repeat open-heart surgeries; therapies advancing along their adoption curves; clinical outcomes; demand of therapies for patients; and other statements that are not historical facts. No inferences or assumptions should be made from statements of past performance, e orts, or results which may not be indicative of future performance or results. 6
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Forward-looking statements are based on estimates and assumptions made by management of the company and are believed to be reasonable, though they are inherently uncertain, di cult to predict, and may be outside of the company’s control. The company's forward-looking statements speak only as of the date on which they are made and the company does not undertake any obligation to update any forward-looking statement to re ect events or circumstances after the date of the statement, except as required by law. If the company does update or correct one or more of these statements, investors and others should not conclude that the company will make additional updates or corrections. Forward-looking statements involve risks and uncertainties that could cause actual results or experience to di er materially from that expressed or implied by the forward-looking statements. Factors that could cause actual results or experience to di er materially from that expressed or implied by the forward-looking statements include: risks related to the failure to successfully innovate and market our products; unsuccessful clinical trials or procedures; manufacturing, logistics or quality issues; competition; dependence on key physicians, research institutions and hospital systems; risks associated with global, economic, political and social conditions; risks related to our international operations; inability to obtain governmental reimbursement or reductions in reimbursement levels; inability to protect our intellectual property; reduced access and demand for our products as a result of, and compliance with, health care legislation and other government regulations; risks related to domestic and foreign income and non-income taxes; use of products in unapproved circumstances and the risk and uncertainties associated with the risks detailed in the company's lings with the Securities and Exchange Commission (SEC), including its Annual Report on Form 10-K for the year ended December 31, 2025, and its other lings with the SEC. These lings, along with important safety information about our products, may be found at edwards.com. Edwards, Edwards Lifesciences, the stylized E logo, AUTUS, Capture Clarity, CLASP, CLASP II, EARLY TAVR, ECLIPTIS, ENCIRCLE, EVOQUE, PASCAL, PASCAL Ace, PASCAL Precision, PROGRESS, RESILIA, SAPIEN, SAPIEN 3, SAPIEN 3 Ultra, SAPIEN M3, TRISCEND, and TRISCEND II are trademarks of Edwards Lifesciences Corporation or its a liates. All other trademarks are the property of their respective owners. ____________________[1]Reported sales and diluted EPS are from continuing operations.[2]The company uses the terms “adjusted” and “constant currency” when referring to non-GAAP sales from continuing operations and sales growthinformation, respectively, which excludes currency exchange rate uctuations and newly acquired products. Adjusted earnings per share fromcontinuing operations is a non-GAAP item computed on a diluted basis and in this press release also excludes certain litigation (insurancerecovery) expenses, net, amortization of intangible assets, restructuring expenses, acquisition contract termination costs, impairment of intangibleand long-lived assets, unrealized gain on marketable securities, gain on remeasurement of previously held interest upon business combinations,fair value adjustments to contingent consideration liabilities, separation costs, loss on impairment, and impact of tax law change on R&D credit.See “Non-GAAP Financial Information” and reconciliation tables below.[3]Represents “adjusted” revenues excluding $2.9 million of revenues related to Implantable Heart Failure Management for the third quarter of 2026.Refer to "Reconciliation of Sales by Product Group and Region" table. 7
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EDWARDS LIFESCIENCES CORPORATIONUnaudited Consolidated Statements of Operations (in millions, except per share data) Three Months EndedSeptember 30,Nine Months EndedSeptember 30, 2026 2025 2026 2025 Net sales $ 1,715.5$ 1,553.1$ 5,105.1$ 4,498.0 Cost of sales 369.2 345.2 1,124.2991.2 Gross pro t 1,346.31,207.93,980.93,506.8Selling, general, and administrative expenses560.9 514.6 1,644.31,482.3Research and development expenses281.4 280.7 823.6 811.5Certain litigation (insurance recovery) expenses, net(12.7) 90.4 30.7 116.8Change in fair value of contingent consideration liabilities— (12.5) — (12.5)Restructuring charges, separation costs, and other10.7 0.1 10.7 8.5Impairment of intangible and long-lived assets220.2 40.0 220.2 40.0 Other operating income (13.3) (12.5) (38.5) (52.9) Operating income, net 299.1 307.1 1,289.91,113.1Interest income, net (36.5) (38.6) (100.0) (112.5)Loss on impairment — — 163.6 47.1 Other non-operating income, net(27.6) (2.7) (115.7) (4.0) Income from continuing operations before provision for income taxes363.2 348.4 1,342.01,182.5 Provision for income taxes 61.8 56.1 418.5 190.7 Net income from continuing operations301.4 292.3 923.5 991.8 Loss from discontinued operations, net of tax— (2.0) — (13.6) Net income 301.4 290.3 923.5 978.2 Net loss attributable to noncontrolling interest(6.1) (0.8) (6.6) (4.1) Net income attributable to Edwards Lifesciences Corporation$ 307.5$ 291.1$ 930.1$ 982.3 Earnings per share: Basic:Continuing operations $ 0.53$ 0.50$ 1.61$ 1.70Discontinued operations $ —$ —$ —$ (0.02)Basic earnings per share $ 0.53$ 0.50$ 1.61$ 1.68Diluted:Continuing operations $ 0.53$ 0.50$ 1.61$ 1.70Discontinued operations $ —$ —$ —$ (0.03)Diluted earnings per share$ 0.53$ 0.50$ 1.61$ 1.67 Weighted-average common shares outstanding: Basic 576.3 584.7 577.3 586.2Diluted 577.6 585.7 578.6 587.2 Operating statistics from continuing operations As a percentage of net sales:Gross pro t 78.5% 77.8% 78.0% 78.0%Selling, general, and administrative expenses32.7% 33.1% 32.2% 33.0%Research and development expenses16.4% 18.1% 16.1% 18.0%Operating income 17.4% 19.8% 25.3% 24.7%Income before provision for income taxes21.2% 22.4% 26.3% 26.3%Net income from continuing operations17.6% 18.8% 18.1% 22.0%E ective tax rate 17.0% 16.1% 31.2% 16.1%____________________Note: Numbers may not calculate due to rounding. EDWARDS LIFESCIENCES CORPORATION Non-GAAP Financial Information To supplement the consolidated nancial results prepared in accordance with Generally Accepted Accounting Principles (“GAAP”), the company uses non-GAAP historical nancial measures. Management makes adjustments to the GAAP measures for items (both charges and gains) that (a) do not re ect the core operational activities of the Company, (b) are commonly adjusted within the Company’s industry to enhance comparability of the Company’s nancial results with those of its peer group, or (c) are inconsistent in amount or frequency between periods (albeit such items are monitored and controlled with equal diligence relative to core operations). The Company uses the 8
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terms “adjusted” and “constant currency” when referring to non-GAAP sales from continuing operations and sales growth information, respectively, which excludes currency exchange rate uctuations and newly acquired products. The Company uses the term “adjusted” to also exclude certain litigation (insurance recovery) expenses, net, amortization of intangible assets, restructuring expenses, acquisition contract termination costs, impairment of intangible and long-lived assets, unrealized gain on marketable securities, gain on remeasurement of previously held interest upon business combinations, fair value adjustments to contingent consideration liabilities, separation costs, loss on impairment, and impact of tax law change on R&D credit. Management uses non-GAAP nancial measures internally for strategic decision making, forecasting future results, and evaluating current performance. These non-GAAP nancial measures are used in addition to, and in conjunction with, results presented in accordance with GAAP and re ect an additional way of viewing aspects of the Company's operations by investors that, when viewed with its GAAP results, provide a more complete understanding of factors and trends a ecting the Company's business and facilitate comparability to historical periods. Non-GAAP nancial measures are not prepared in accordance with GAAP; therefore, the information is not necessarily comparable to other companies and should be considered as a supplement to, and not as a substitute for, or superior to, the corresponding measures calculated in accordance with GAAP. A reconciliation of non-GAAP historical nancial measures to the most comparable GAAP measure is provided in the tables below. Fluctuations in currency exchange rates impact the comparative results and sales growth rates of the Company's underlying business. Management believes that excluding the impact of currency exchange rate uctuations from its sales growth provides investors a more useful comparison to historical nancial results. The impact of the uctuations has been detailed in the “Reconciliation of Sales by Product Group and Region.” Guidance for sales and sales growth rates is provided on a “constant currency basis,” and projections for diluted earnings per share, net income and growth, gross pro t margin, and taxes are also provided on a non-GAAP basis, as adjusted, for the items identi ed above due to the inherent di culty in forecasting such items without unreasonable e orts. The Company is not able to provide a reconciliation of the non-GAAP guidance to comparable GAAP measures due to the unknown e ect, timing, and potential signi cance of special charges or gains, and management's inability to forecast charges associated with future transactions and initiatives. The items described below are adjustments to the GAAP nancial results in the reconciliations that follow: Certain Litigation (Insurance Recovery) Expenses, net - The Company incurred certain litigation expense of $37.1 million and $10.9 million in the rst quarter of 2026 and 2025, respectively, $6.3 million and $15.5 million 9
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for the second quarter of 2026 and 2025, respectively, and a net insurance recovery of $12.7 million and certain litigation expenses of $90.4 million in the third quarter of 2026 and 2025, respectively. Such amounts relate to intellectual property litigation, settlements, contingencies, external legal costs, and associated insurance recoveries. Amortization of Intangible Assets - The Company recorded amortization expense related to developed technology and patents in the amount of $3.3 million and $1.4 million in the rst quarter of 2026 and 2025, respectively, $3.2 million and $1.8 million in the second quarter of 2026 and 2025, respectively, and $3.2 million and $1.7 million in the third quarter of 2026 and 2025, respectively. Restructuring Expenses - The Company recorded a $2.0 million charge in the third quarter of 2026 related to severance expense associated with realignment initiatives. Acquisition Contract Termination Costs - The Company recorded expenses of $8.7 million in the third quarter of 2026 related to the termination of certain contracts associated with the Company's acquisitions. Separation Costs - The Company recorded expenses of $4.2 million in both the rst and second quarter of 2025 and $0.1 million in the third quarter of 2025 related to consulting, legal, tax, and other professional advisory services related to the sale of Critical Care. Impairment of Intangible and Long-Lived Assets - The Company recorded a $220.2 million charge in the third quarter of 2026 related to impairment of a certain in-process research and development asset and xed assets acquired as part of an acquisition. The Company recorded a $40.0 million charge in the third quarter of 2025 related to an impairment of a certain developed technology asset acquired as part of an acquisition. Unrealized Gain on Marketable Securities - The Company recorded an unrealized gain of $19.1 million in the third quarter of 2026 related to changes in the fair value of its marketable equity securities. Gain on Remeasurement of Previously Held Interest Upon Business Combinations - The Company recorded a $65.2 million gain in the rst quarter of 2026 to remeasure its previously held interest upon acquisition of an investee and a $19.9 million gain in the second quarter of 2026 to remeasure its previously held interest upon consolidation of one of its variable interest entities (“VIE”). Change in Fair Value of Contingent Consideration Liabilities - The Company recorded a gain of $12.5 million in the third quarter of 2025 related to changes in the fair value of its contingent consideration liabilities arising from acquisitions. Loss on Impairment - The Company recorded a loss on impairment of $123.6 million in the rst quarter of 2026 10
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due to the carrying amount of one of its VIE investments not being recoverable and $40.0 million in the second quarter of 2026 due to the Company's determination to not exercise an option to acquire one of its VIEs. The Company recorded loss on impairment of $47.1 million in the second quarter of 2025, related to the Company's determination to not exercise an option to acquire one of its VIE investments. Impact of Tax Law Change on R&D Credit - The Company recorded a $174.4 million valuation allowance against certain deferred tax assets in 2026. The Company established the valuation allowance due to California budget legislation enacted on June 29, 2026 which includes a new permanent limitation that applies to most business tax credits including carryovers of research and development tax credits. Provision for Income Taxes - The income tax impacts of the expenses and gains discussed above are based upon the items' forecasted e ect upon the Company's full-year e ective tax rate. Adjustments to forecasted items unrelated to the expenses and gains above, as well as impacts related to interim reporting, will have an e ect on the income tax impact of these items in subsequent periods. EDWARDS LIFESCIENCES CORPORATIONUnaudited Reconciliation of GAAP to Non-GAAP Financial Information(in millions, except per share and percentage data)Three Months Ended September 30, 2026 NetSales GrossPro tMargin OperatingIncome,net OperatingPro tMargin OtherNon-operatingIncomeNetIncomeDilutedEPSE ectiveTax RateGAAP - ContinuingOperations$ 1,715.578.5%$ 299.117.4%$ 27.6$ 301.4$ 0.53 17.0%Net loss attributable tononcontrolling interests— — — — — 6.1 — — Total attributable to EdwardsLifesciences Corporation1,715.578.5% 299.117.4% 27.6 307.5 0.53 17.0%Non-GAAP adjustments:(A) (B)Certain litigation insurancerecovery, net — — (12.7) (0.7) — (10.3) (0.02) (0.1)Amortization of intangibleassets — 0.2 3.2 0.2 — 2.3 — 0.1Restructuring expenses— — 2.0 0.1 — 1.8 — —Acquisition contracttermination costs— — 8.7 0.5 — 7.8 0.02 (0.1)Impairment of intangible andlong-lived assets— — 220.212.8 — 185.4 0.33 (0.3)Unrealized gain on marketablesecurities — — — — (19.1) (14.7) (0.03) (0.2)Prior period ongoing taximpacts — — — — — (20.4) (0.03) 3.4 Adjusted $ 1,715.578.7%$ 520.530.3%$ 8.5$ 459.4$ 0.80 19.8% Three Months Ended September 30, 2025 GrossOperatingOperatingOtherNon- 11
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NetSales GrossPro tMargin OperatingIncome,net OperatingPro tMargin NonoperatingIncomeNetIncomeDilutedEPSE ectiveTax RateGAAP - ContinuingOperations$ 1,553.177.8%$ 307.119.8%$ 2.7$ 292.3$ 0.50 16.1%Net loss attributable tononcontrolling interests— — — — — 0.8 — — Total attributable to EdwardsLifesciences Corporation1,553.177.8% 307.119.8% 2.7 293.1 0.50 16.1%Non-GAAP adjustments:(A) (B)Certain litigation expenses— — 90.4 5.8 — 69.6 0.12 1.3Amortization of intangible assets— 0.1 1.7 0.1 — 1.3 — —Separation costs— — 0.1 — — — — —Impairment of intangible andlong-lived assets— — 40.0 2.6 — 38.5 0.07 (1.1)Change in fair value ofcontingent considerationliabilities — — (12.5) (0.8) — (12.0) (0.02) 0.4 Prior period ongoing tax impacts— — — — — (0.6) — 0.2 Adjusted $ 1,553.177.9%$ 426.827.5%$ 2.7$ 389.9$ 0.67 16.9% Nine Months Ended September 30, 2026 NetSales GrossPro tMarginOperatingIncome OperatingPro tMarginLoss onImpairment OtherNon-operatingIncomeNetIncomeDilutedEPSE ectiveTax RateGAAP - ContinuingOperations$5,105.178.0%$ 1,289.925.3%$ 163.6$ 115.7$ 923.5$ 1.6131.2%Net loss attributable tononcontrolling interests— — — — — — 6.6 — — Total attributable to EdwardsLifesciences Corporation5,105.178.0% 1,289.925.3% 163.6115.7930.11.6131.2%Non-GAAP adjustments:(A) (B)Certain litigation expenses,net — — 30.7 0.6 — — 22.3 0.03 (0.1)Amortization of intangibleassets — 0.2 9.7 0.2 — — 7.3 — (0.1)Restructuring expenses— — 2.0 — — — 1.8 — —Acquisition contracttermination costs— — 8.7 0.2 — — 7.8 0.02 (0.1)Impairment of intangibleand long-lived assets— — 220.24.3 — — 185.40.33 (1.8)Unrealized gain onmarketable securities— — — — — (19.1) (14.7) (0.03) 0.1Gain on remeasurement ofpreviously held interestupon businesscombinations— — — — — (85.1) (77.4) (0.13) 1.2Loss on impairment— — — — (163.6) — 125.50.22 (0.7)Impact of tax law change onR&D credit — — — — — — 174.40.30(10.8) Adjusted$5,105.178.2%$ 1,561.230.6%$ —$ 11.5$1,362.5$ 2.3518.9% Nine Months Ended September 30, 2025 NetSales GrossPro tMarginOperatingIncome OperatingPro tMarginLoss onImpairment OtherNon-operatingIncomeNetIncomeDilutedEPSE ectiveTax RateGAAP - ContinuingOperations$4,498.078.0%$1,113.124.7%$ 47.1$ 4.0$ 991.8$ 1.7016.1%Net loss attributable tononcontrolling interests— — — — — — 4.1 — — Total attributable to EdwardsLifesciences Corporation4,498.078.0% 1,113.124.7% 47.1 4.0995.91.7016.1%NGAAPdjt t(A)(B) 12
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Non-GAAP adjustments:(A) (B)Certain litigation expenses— — 116.8 2.6 — — 90.4 0.16 0.4Amortization of intangibleassets — 0.1 4.9 0.1 — — 3.9 — —Separation costs— — 8.5 0.2 — — 6.6 0.01 0.1Impairment of intangibleand long-lived assets— — 40.0 1.0 — — 38.5 0.07 (0.2)Change in fair value ofcontingent considerationliabilities — — (12.5) (0.3) — — (12.0) (0.02) 0.1Loss on impairment— — — — (47.1) — 37.6 0.06 0.1Prior period ongoing taximpacts — — — — — — (0.6) — 0.1 Adjusted$4,498.078.1%$1,270.828.3%$ —$ 4.0$1,160.3$ 1.9816.7% ____________________(A)See description of non-GAAP adjustments under “Non-GAAP Financial Information.”(B)The tax e ect on non-GAAP adjustments is calculated based upon the impact of the relevant tax jurisdictions’ statutory tax rates on the Company’sestimated annual e ective tax rate, or discrete rate in the quarter, as applicable. The impact on the e ective tax rate is re ected on each individualnon-GAAP adjustment line item. RECONCILIATION OF SALES BY PRODUCT GROUP AND REGION2025 Adjusted Sales by Product Group (QTD) -Continuing Operations3Q 20263Q 2025Change GAAPGrowthRate*FXImpact 3Q 2025AdjustedSales ConstantCurrencyGrowthRate * Transcatheter Aortic ValveReplacement $ 1,241.6$ 1,149.9$ 91.7 8.0%$ (7.9) $ 1,142.08.8% Transcatheter Mitral and TricuspidTherapies(A) 209.5145.264.344.3% (1.5) 143.745.9% Surgical(B) 264.4258.0 6.4 2.5% (0.4) 257.62.8% Total $1,715.5$1,553.1$162.410.5%$ (9.8)$1,543.311.2% 2025 Adjusted Sales by Product Group (YTD) -Continuing OperationsYTD 3Q2026YTD 3Q2025Change GAAPGrowthRate*FXImpact YTD 3Q2025AdjustedSales ConstantCurrencyGrowthRate * Transcatheter Aortic Valve Replacement$ 3,697.2$ 3,327.4$ 369.811.1%$ 32.5$ 3,359.910.1% Transcatheter Mitral and TricuspidTherapies(A) 583.2394.9188.347.7% 8.3 403.244.7% Surgical(B) 824.7775.749.0 6.3% 13.4 789.14.6% Total $5,105.1$4,498.0$607.113.5%$ 54.2$4,552.212.2% 2025 Adjusted GAAP 3Q2025ConstantCurrency 13
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Sales by Region (QTD) - ContinuingOperations 3Q20263Q2025Change GAAPGrowthRate*FXImpact 3Q 2025AdjustedSales CurrencyGrowthRate * United States $1,007.6$907.5$100.111.0%$ —$907.511.0% Europe 414.6387.926.7 6.9% (4.3) 383.68.2%Japan 92.0 90.1 1.9 2.2% (8.1) 82.012.2% Rest of World 201.3167.633.720.2% 2.6 170.218.3% Outside of the United States707.9645.662.39.7% (9.8) 635.811.5% Total $1,715.5$1,553.1$162.410.5%$ (9.8)$1,543.311.2% 2025 Adjusted Sales by Region (YTD) - ContinuingOperations YTD 3Q2026YTD 3Q2025Change GAAPGrowthRate*FXImpact YTD 3Q2025AdjustedSales ConstantCurrencyGrowthRate * United States $2,948.7$2,636.1$312.611.9%$ —$2,636.111.9% Europe 1,296.81,107.9188.917.0% 54.01,161.911.6%Japan 279.0267.211.8 4.4% (16.8) 250.411.4% Rest of World 580.6486.893.819.3% 17.0 503.815.3% Outside of the United States2,156.41,861.9294.515.8% 54.21,916.112.6% Total $5,105.1$4,498.0$607.113.5%$ 54.2$4,552.212.2% ____________________(A)Revenues related to Implantable Heart Failure Management of $2.9 million and $1.7 million for the third quarter of 2026 and 2025, respectively,and $7.6 million and $3.6 million for year-to-date 2026 and 2025, respectively, were included in TMTT sales.(B)Revenues related to a transitional service agreement from 2025 sale of our non-product group of $1.5 million and $6.8 million for third quarter of2026 and year-to-date 2026, respectively, were included in Surgical sales.*Numbers may not calculate due to rounding. Media: Eric Endicott, media@edwards.com Investors: Gerianne Sarte, investor_relations@edwards.com Source: Edwards Lifesciences Corporation 14