AI
AtriCure, Inc. (ATRC)·Q4 2024 Earnings Summary
Executive Summary
- Q4 2024 revenue was $124.3M, up 16.6% YoY, with U.S. $101.6M (+14.4%) and International $22.7M (+27.7%); gross margin was 74.5% and adjusted EBITDA improved to $12.7M while GAAP EPS was a loss of $0.33 and adjusted loss per share was $0.08 .
- Sequentially, revenue grew $8.4M (+7.2%) versus Q3, driven by cryoSPHERE pain management, AtriClip FLEX-V in appendage management, and EnCompass clamp adoption; International growth outpaced U.S. .
- 2025 guidance: revenue $517–$527M (maintained), adjusted EBITDA raised to $42–$44M (from $40–$44M in Jan.), adjusted loss per share $0.57–$0.64, gross margin expected ~flat vs 2024; modest positive cash generation anticipated .
- Near-term catalysts: March 26 Analyst & Investor Day (pipeline, PFA roadmap, long-term financial goals), CE-Mark launch of EnCompass in Europe, and U.S. launches of cryoSPHERE+ and cryoSPHERE MAX and AtriClip FLEX-Mini .
What Went Well and What Went Wrong
What Went Well
- Pain management accelerated: franchise grew 32% in 2024 and 43% in Q4; cryoSPHERE+ and cryoSPHERE MAX reduced freeze times by 25–50%, improving adoption. “These probes reduced freeze times by 25% to 50%… resulting in a meaningful overall reduction in cryo nerve block therapy procedure time” (CEO) .
- Open ablation momentum: EnCompass drove >50% growth within open ablation in Q4; “pretty much all of the growth…is from net new users or an expansion of use” (CEO) .
- Appendage management strength: U.S. open AtriClip devices up ~20% in Q4 with FLEX-Mini launch; China approval and CE-mark indication expansion support multi-year tailwinds .
What Went Wrong
- U.S. minimally invasive (MIS) pressure: hybrid ablation and MIS AtriClip devices expected to decline in 2025 due to PFA adoption; management assumes no YoY growth for these categories in the U.S. (CFO) .
- Mix-driven margin headwinds: gross margin fell YoY to 74.5% in Q4 due to less favorable product/geography mix; rebasing around ~75% for 2025 (CFO) .
- One-time IPR&D expense: $12M upfront PFA licensing payment lifted R&D to $35.0M in Q4 and widened GAAP loss; adjusted EBITDA/LPS exclude acquired IPR&D going forward .
Financial Results
Summary Metrics (Quarterly)
Notes:
- Sequential revenue growth +7.2% in Q4 vs Q3 (CFO commentary) .
- Q4 GAAP loss driven by $12M acquired IPR&D; non-GAAP metrics exclude IPR&D hence improved adjusted results .
Segment Breakdown – United States Revenue ($USD Thousands)
Segment Breakdown – International Revenue ($USD Thousands)
KPIs and Operating Expenses ($USD Thousands)
Guidance Changes
Earnings Call Themes & Trends
Management Commentary
- “These probes reduced freeze times by 25% to 50%… resulting in a meaningful overall reduction in cryo nerve block therapy procedure time” (CEO on cryoSPHERE+ and MAX) .
- “We are pretty much through most of the PFA piece [in Europe]… growth to over 20% this year in the Convergent area… we do anticipate that dynamic… in the United States” (CEO on MIS/PFA) .
- “Rebasing around a 75% gross margin… relatively flat [2025]” (CFO) .
- “We now expect full year 2025 adjusted EBITDA to range from $42M to $44M” (CFO) .
- “We do anticipate… PMA… [PFA] will go into EnCompass Clamp and EPi-Sense… we’ll roll out more granular timeline at the Analyst Day” (CEO) .
Q&A Highlights
- EnCompass growth is driven by net-new users and expanded use rather than conversion; CABG market unlocked (CEO) .
- U.S. MIS ablation and MIS AtriClip expected to decline in 2025; improvement potential in 2H as PFA dynamics normalize (CFO) .
- International profitability headwind to gross margin offset by U.S. new product margins and manufacturing efficiencies (CFO) .
- FLEX-Mini conversion timeline is multi-year, similar to FLEX-V adoption curve (CFO) .
- LeAAPS enrollment targeted for completion in 2025; event-driven design likely requires full follow-up for readout (CEO) .
Estimates Context
- Wall Street consensus estimates via S&P Global were unavailable at the time of review due to API request limits; therefore, comparisons vs consensus for Q4/Q3/Q2 EPS, revenue, and EBITDA are not included. Values would normally be retrieved from S&P Global; data was unavailable.
- Modeling implications: rebase gross margin to ~75% in 2025, assume U.S. MIS and MIS AtriClip declines, and integrate raised adjusted EBITDA floor to $42–$44M; Q1 2025 revenue cadence likely flat vs Q4 2024 (CFO) .
Key Takeaways for Investors
- Mixed but constructive print: double-digit revenue growth and improved adjusted EBITDA, with GAAP loss widened by one-time IPR&D; non-GAAP excludes IPR&D going forward .
- Product cycle strength: cryoSPHERE+ and MAX plus FLEX-Mini are early but potent adoption drivers; expect multi-year contribution and potential pricing/mix benefits (CFO/CEO) .
- Open ablation runway: EnCompass adoption remains robust with Europe launch; growth is net-new usage, not just replacement—sustained tailwind into 2025+ .
- MIS near-term headwind: U.S. hybrid/MIS AtriClip under pressure from PFA; management bakes in declines for 2025—watch for inflection late 2025/2026 as non-responders funnel to Convergent .
- Margins stable: rebase GM ~75% with OUS mix headwind offset by U.S. new product margins and manufacturing efficiencies; model flat GM in 2025 (CFO) .
- 2025 outlook: revenue $517–$527M (maintained); adjusted EBITDA raised to $42–$44M; adjusted LPS $0.57–$0.64; Q1 cadence flat to Q4 .
- Near-term catalysts: March 26 Analyst Day for PFA PMA path, BoxX-NoAF trial details, long-term financial goals; continued OUS expansion with CE-marked EnCompass .