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AtriCure, Inc. (ATRC)·Q2 2025 Earnings Summary
Executive Summary
- Q2 2025 delivered a beat-and-raise: revenue $136.1M (+17.1% YoY) and adjusted EPS loss of $0.02, with adjusted EBITDA $15.4M and cash generation of $17.9M; guidance increased for FY25 revenue and adjusted EBITDA .
- Versus Wall Street: revenue beat consensus by ~$5.9M ($136.1M vs $130.3M*) and adjusted EPS loss of $0.02 beat consensus loss of ~$$0.163*; 8 estimates for both metrics* .
- Strong franchise performance: U.S. pain management +41% YoY, U.S. open appendage management +30% YoY; international revenue +23% with broad-based strength .
- Strategic milestones: completed enrollment (6,500 patients) in LeAAPS stroke-prevention trial; PFA-enabled Encompass platform progressed toward first-in-human; CryoXT amputation pain device poised for launch later in 2025 .
What Went Well and What Went Wrong
What Went Well
- Robust top-line and profitability: “outstanding second quarter with total revenue of $136 million… over $15 million in adjusted EBITDA and nearly $18 million in cash generation” .
- Product-led acceleration: “new product launches such as AtriClip FLEX-Mini and cryoSPHERE MAX drove accelerated growth” in appendage management and pain management .
- Clinical execution: “completed enrollment earlier this month” in LeAAPS, the largest cardiac surgery device trial ever, and BoxX-NoAF site activation is underway .
What Went Wrong
- Minimally invasive hybrid therapy headwinds: U.S. MIS ablation declined to $7.8M due to PFA catheter adoption; management expects continued modest sequential declines in the hybrid franchise through 2025 .
- Gross margin mix pressure: GM 74.5%, down ~15 bps YoY on less favorable geographic/product mix, largely international .
- Operating expense step-up: total OpEx +14.5% YoY to $107.7M, including a $5M PFA milestone; excluding milestone, OpEx +9.2% YoY, reflecting R&D and clinical investment .
Financial Results
Core Financials vs prior quarters
Additional datapoints:
- Sequential revenue growth: +10.1% vs Q1 2025 .
- Cash generation: $17.9M in Q2 (includes PFA milestone payment) .
Segment and Geography Breakdown (Q2 2025 vs Q2 2024)
Notable call commentary:
- U.S. open appendage management growth +30% (FLEX-Mini adoption ~20% of U.S. appendage revenue) .
- CryoSPHERE MAX contributed just over 50% of U.S. pain management sales; MAX in a little over half of U.S. accounts .
- International revenue +23.3% reported (+19.9% cc), with Europe $16.1M (+27.7%) and APAC/Other $9.4M (+16.3%) .
Estimates vs Actual (S&P Global; Q2 2025)
- Revenue - # of Estimates: 8*; Primary EPS - # of Estimates: 8*.
- Values retrieved from S&P Global.*
Guidance Changes
Drivers:
- Strength in pain management and appendage management, ongoing Encompass adoption; international outpacing U.S.; hybrid MIS expected to remain pressured by PFA catheter adoption .
Earnings Call Themes & Trends
Management Commentary
- CEO: “new product launches such as AtriClip FLEX-Mini and cryoSPHERE MAX drove accelerated growth… first lower limb amputation procedures using our CryoXT device… we began testing our PFA device for cardiac surgery” .
- CEO on market runway: CABG patient penetration moving toward 80–90% in AFib-only patients over time; BoxX-NoAF could triple the market; “more than a decade worth of really strong growth sitting in front of us” .
- CFO: “Gross margin was 74.5%… decrease primarily driven by less favorable geographic and product mix… total operating expenses included a $5 million milestone payment under the PFA co-development agreement” .
- CFO on outlook: FY25 revenue $527–$533M; adjusted EBITDA $49–$52M; adjusted LPS $(0.34)–$(0.39); Q3 seasonality down low single digits sequentially, rebound in Q4 .
Q&A Highlights
- Appendage management utilization post-LeAAPS: Trial completion has “zero impact” on revenue; overall adoption rising; competition has increased awareness, aiding AtriClip growth .
- MIS hybrid therapy: Pressure from PFA persists; management sets expectations low for near-term recovery while other franchises more than offset headwinds .
- Pain management drivers: MAX cut freeze time (2 min to 1 min), enabling procedural throughput; volume growth a little over 30% with pricing uplift; strong new account adoption .
- CryoXT launch: Minimal 2025 revenue contribution; learning-focused rollout for a bigger 2026 impact .
- PFA clamp differentiation: Combining PFA + RF in one Encompass clamp with single generator; ergonomic and time-saving benefits .
- SG&A cadence: Expect mid-to-upper single-digit growth, below top-line, reflecting scale efficiencies .
Estimates Context
- Q2 2025 beat: revenue $136.1M vs consensus $130.3M*; adjusted Primary EPS $(0.02)* vs $(0.163); both based on 8 estimates .
- Implications: Consensus likely to move higher for FY25 revenue and EBITDA after raised guidance; hybrid MIS assumptions should remain conservative given management commentary .
- Values retrieved from S&P Global.*
Key Takeaways for Investors
- Beat-and-raise quarter driven by product leadership; near-term catalysts include CryoXT launch learning-cycle in 2H and first-in-human PFA Encompass by year-end .
- Pain management is a secular growth engine with strong volume and pricing mix from MAX; expect above-company growth in 2H though comps toughen .
- Appendage management momentum accelerating (FLEX-Mini, PRO-Mini), with competition expanding awareness and AtriCure’s clinical evidence strategy underpinning sustained share .
- Hybrid MIS remains a drag; model it cautiously with continued sequential pressure through FY25, while open ablation and appendage management offset .
- International expansion is broad-based and outpacing U.S.; monitor GM impact from geographic/product mix .
- LeAAPS completion is a strategic inflection—follow-up milestones and eventual data could expand indications and guidelines; BoxX-NoAF site activations broaden TAM over time .
- Near-term trading catalyst: sustained execution with typical Q3 seasonality and Q4 rebound; consensus upgrades likely around raised FY25 revenue/EBITDA and continuing franchise strength .
Additional Relevant Press Releases
- LeAAPS enrollment completion (6,500 patients; largest cardiac surgery device trial): reinforces strategic clinical evidence plan and potential guideline impact .
- CryoXT device launch (post-amputation pain; announced Sep 9, 2025): validates call commentary on initial procedures and sets stage for 2026 revenue contribution .
Non-GAAP notes:
- Adjusted EBITDA excludes items such as acquired IPR&D/milestone payments (e.g., $5M PFA milestone in Q2) and share-based compensation; adjusted EPS excludes non-cash/fair value and certain one-time items; reconciliations provided in 8-K .
Footnote: Values marked with * are retrieved from S&P Global.