Edwards Lifesciences earnings date
Edwards Lifesciences (EW) Q3 2026 Earnings Report
CH:EW Q3 2026 EPS Results
- Actual EPS
- CHF 0.67
- Consensus EPS
- CHF 0.62
- Beat/Miss
- Beat by +CHF 0.05
- One Year Ago EPS
- CHF 0.56
CH:EW Q3 2026 Revenue Results
- Actual Revenue
- CHF 1.43B
- Expected Revenue
- CHF 1.40B
- Beat/Miss
- Beat by +CHF 29.46M
- YoY Revenue Growth
- +10.46%
Earnings Announcement Details
- Quarter
- Q3 2026
- Date
- 11/04/2026
- Time
- After Close
- Conference Call
- Wednesday, November 4, 2026
Edwards Lifesciences's next earnings date is estimated for January 27, 2027, based on past reporting schedules.
Q3 2026 Earnings Call Audio
Q3 2026 Earnings Slide Deck
No slide deck is available for this earnings event.
Q3 2026 Earnings Call Summary
The call was strongly positive. Edwards reported better-than-expected third-quarter results, raised full-year sales, TAVR, TMTT and EPS guidance, highlighted broad clinical and regulatory progress, and expressed confidence in durable long-term growth. The main challenges were GAAP EPS impairment, foreign-exchange and tax headwinds, expected fourth-quarter margin phasing, moderating TAVR share gains and the gradual timing of new-indication benefits.
Management raised full-year 2026 total sales growth guidance to approximately 11.5% and adjusted EPS guidance to $2.97 to $3.05, growing 18% at the midpoint versus prior year; fourth-quarter sales are projected at $1.67 billion to $1.75 billion with adjusted EPS of $0.61 to $0.69. Full-year TAVR guidance is 9% to 9.5%, with durable mid- to high single-digit growth over the long term; TMTT sales are expected to be between $780 million and $790 million, supporting a path to $2 billion in TMTT revenue in 2030; and Surgical guidance remains mid-single-digit sales growth. Adjusted gross margin is expected at the lower end of the full year 78% to 79% gross margin guidance, operating margin at the high end of the original 28% to 29% guidance with approximately 150 basis points of constant currency operating margin expansion, fourth-quarter operating margin in the mid-20s, R&D expense at approximately 16.5% of sales, effective tax rate at the high end of 16% to 19%, fourth-quarter FX headwind of approximately $15 million, and average diluted shares outstanding between 575 million and 580 million; beyond 2026, Edwards plans for 50 to 100 basis points of underlying operating margin expansion and approximately 10% average annual sales growth alongside leveraged EPS growth.
- Strong Third-Quarter Company PerformanceThird-quarter sales were $1.72 billion, growing 11.2% year-over-year and exceeding expectations, with broad-based performance across businesses and regions. Adjusted EPS was $0.80.
- Raised Full-Year Company GuidanceBased on third-quarter performance, Edwards raised full-year sales growth guidance to approximately 11.5% and adjusted EPS guidance to $2.97 to $3.05, representing 18% EPS growth at the midpoint versus the prior year.
- Long-Term Growth Framework ReaffirmedManagement reaffirmed its long-term target of approximately 10% average annual sales growth alongside leveraged EPS growth, supported by multiyear opportunities across structural heart.
- Clinical, Regulatory and Commercial MilestonesThe company reported 5 meaningful therapy approvals in recent months and the release of 2 new practice-changing data sets. Management said these milestones strengthened the outlook for durable long-term growth.
- TAVR Revenue Growth and Competitive PositionThird-quarter global TAVR sales were $1.2 billion, increasing 8.8% year-over-year and coming in stronger than expected. Growth rates were similar in the U.S. and outside the U.S., average selling prices were stable globally, and competitive position increased modestly year-over-year in the U.S. and Europe.
- Raised Full-Year TAVR GuidanceFull-year TAVR sales growth guidance was raised to 9% to 9.5%. Management expects future growth to be driven mainly by continued increases in procedure volume and less by share gains.
- Positive TAVR Procedure TrendsManagement reported encouraging signs of procedure growth exiting the third quarter, including an early positive procedure signal in the last few weeks of the quarter. The company said the heightened focus on TAVR, clinical evidence and the updated NCD were having an impact on the market.
- PROGRESS Trial Advances Moderate Aortic Stenosis CareThe PROGRESS trial met a major clinical milestone, with results presented at TCT and published in the New England Journal of Medicine. Management said the results challenge passive surveillance for moderate aortic stenosis patients with at-risk features and support earlier referral and proactive disease management.
- Large Moderate Aortic Stenosis OpportunityThe ACTIVATE real-world study included more than 53,000 patients with aortic stenosis and found that moderate AS patients outnumbered severe AS patients nearly 2:1. Approximately 80% of moderate AS patients had at least one at-risk feature associated with increased risk of death and hospitalization.
- Additional Evidence Supporting Earlier TAVRLong-term economic data from EARLY TAVR showed exceptional economic value versus clinical surveillance in asymptomatic severe AS and remained highly cost effective after accounting for potential future valve reintervention. Median time to intervention was 32 days in the trial versus approximately 157 days in real-world practice.
- Updated U.S. TAVR NCD Expands AccessCMS released the final updated NCD for TAVR. Management said it provides greater heart-team flexibility, supports appropriate site expansion through updated hospital procedure volume requirements, expands coverage to asymptomatic patients, and creates a pathway for MAC coverage when future TAVR indications are approved.
- International TAVR AdoptionIn Europe, updated ESC and EACTS guidelines are supporting discussion of earlier intervention and proactive disease management. In Japan, SAPIEN 3 Ultra RESILIA continued to see strong adoption, and dedicated reimbursement was secured for the technology.
- TMTT Sales Increased 45.6%Third-quarter TMTT sales were $207 million, increasing 45.6% year-over-year. Global mitral and tricuspid procedure volumes continued to grow in the double digits, and the U.S. became a more significant driver as it scaled.
- Raised Full-Year TMTT GuidanceFull-year TMTT sales guidance was raised to between $780 million and $790 million. Management said the full portfolio is now available to patients across the U.S. and Europe and supports a path to $2 billion in TMTT revenue in 2030.
- Expanded PASCAL Approvals and Clinical EvidencePASCAL Ace with Capture Clarity received U.S. approval for DMR TEER procedures, and PASCAL Precision for tricuspid regurgitation received U.S. approval. The CLASP II TR pivotal trial met its 6-month primary endpoint, demonstrating superiority of PASCAL plus optimal medical therapy versus optimal medical therapy alone, driven by significant health-status improvements.
- EVOQUE Clinical and Regulatory ProgressEVOQUE delivered another strong quarter of growth. U.S. approval and CE Mark were received for transjugular access, enabling treatment of patients with complex femoral access. In more than 1,100 patients followed for one year in the TVT Registry, EVOQUE showed sustained elimination of TR, quality-of-life improvements, excellent valve durability and a high rate of procedural success.
- Positive Tricuspid Intervention EvidenceThe Edwards-supported TRIC-I-HF study demonstrated a statistically significant reduction in the combined endpoint of heart-failure hospitalization and mortality for tricuspid intervention versus optimal medical therapy at one year.
- SAPIEN M3 ProgressManagement reported strong demand for SAPIEN M3 among patients who are not suitable for mitral TEER. Two-year ENCIRCLE results reinforced durability, sustained reduction of mitral regurgitation, functional improvement and quality-of-life benefits. SAPIEN M3 with RESILIA was introduced in Europe during the quarter.
- Surgical Portfolio Adoption and New ProductsThird-quarter Surgical sales were $264 million, increasing 3% year-over-year, driven by continued adoption of the RESILIA portfolio. AUTUS became the first FDA-approved surgical pulmonary valve designed specifically for pediatric anatomy with the ability to expand as a child grows, and the company advanced the U.S. rollout of ECLIPTIS for surgical left atrial appendage occlusion.
- Improved Gross and Operating MarginsThird-quarter adjusted gross profit margin was 78.7%, compared with 77.9% in the prior year. Adjusted operating profit margin was 30.3%. Management expects full-year operating margin at the high end of the original 28% to 29% guidance, implying approximately 150 basis points of constant-currency operating margin expansion.
- Operating Expense Leverage and Innovation InvestmentSG&A was $561 million, or 32.7% of sales, compared with $515 million, or 33.1% of sales, in the prior year. R&D was $281 million, or 16.4% of sales, compared with 18.1% in the prior year. Management expects R&D expense as a percentage of sales to be approximately 16.5% in 2026 while continuing to invest in the expanding structural-heart portfolio.
- Strong Balance Sheet and Share RepurchasesEdwards had approximately $3.1 billion in cash and cash equivalents as of September 30, 2026. The company repurchased approximately $700 million of shares through the third quarter and had approximately $1.3 billion remaining under its share-repurchase authorization.
- Confidence in Future GrowthManagement expressed confidence in delivering the increased 2026 outlook and in targeting 10% longer-term sales growth on average with EPS leverage. The company said its strategy, clinical evidence and new indications position it for sustainable growth over multiple years.
CH:EW Earnings History
| Report Date | Fiscal Quarter | Forecast / EPS | Last Year's EPS | EPS YoY Change | Press Release |
|---|---|---|---|---|---|
| Jan 27, 2027 | 2026 (Q4) | 0.55- | 0.48 | ― | ― |
| Nov 04, 2026 | 2026 (Q3) | 0.620.67 | 0.56 | 19.40% (+0.11) | |
| Jul 23, 2026 | 2026 (Q2) | 0.620.65 | 0.56 | 16.42% (+0.09) | |
| Apr 23, 2026 | 2026 (Q1) | 0.610.65 | 0.53 | 21.88% (+0.12) | |
| Feb 10, 2026 | 2025 (Q4) | 0.520.48 | 0.49 | -1.69% (-0.01) | |
| Oct 30, 2025 | 2025 (Q3) | 0.500.56 | 0.56 | 0.00% (+0.00) | |
| Jul 24, 2025 | 2025 (Q2) | 0.520.56 | 0.58 | -4.29% (-0.03) | |
| Apr 23, 2025 | 2025 (Q1) | 0.500.53 | 0.55 | -3.03% (-0.02) | |
| Feb 11, 2025 | 2024 (Q4) | 0.460.49 | 0.53 | -7.81% (-0.04) | |
| Oct 24, 2024 | 2024 (Q3) | 0.560.56 | 0.49 | 13.56% (+0.07) |
The table shows recent earnings report dates and whether the forecast was beat or missed. See the change in forecast and EPS from the previous year.

