Every 10-Q that Atricure (ATRC) has filed with the SEC in the last 24 months is listed below, newest first, and each one links through to the document itself with the summary and the scores our analysis gives it.
A 10-Q covers the quarterly report filed between annual reports, so if you follow ATRC and want that one kind of document rather than the whole filing history, this is the page to keep. The company's other filings, of every form, are on the full ATRC filings page.
AtriCure, Inc. reported strong Q1 2026 growth, with revenue of $141,249, up 14.3% from Q1 2025. U.S. sales reached $116,205, led by appendage management and pain management products, while international revenue rose 11.5%.
Gross margin improved to 77.4%, and the company swung from a $6,747 net loss to modest net income of $108. Operating cash outflow improved to $3,996, ending the quarter with $146,165 in cash and $61,000 of debt outstanding.
AtriCure (ATRC) reported solid third‑quarter growth and near break‑even results. Revenue rose to $134,269, up 15.8% year over year, with gross margin at 75.5% versus 74.9% a year ago. Operating income was $208, and net loss narrowed to $267, or $0.01 per share. For the first nine months, revenue reached $394,028, up 15.5%.
Growth was led by appendage management and pain management in the United States, while minimally invasive ablation declined as physicians shifted procedures. Cash and cash equivalents were $147,865 with long‑term debt of $61,865 and unused ABL borrowing availability of $61,885 as of September 30, 2025. The company completed enrollment of 6,500 patients in the LeAAPS trial and launched the cryoICE cryoXT probe for amputation pain therapy in the U.S. A sale‑and‑leaseback of a building resulted in a $6,250 financing obligation. Shares outstanding were 49,716,988 as of October 27, 2025.
AtriCure (ATRC) Q2-25 10-Q highlights: Revenue rose 17.1% YoY to $136.1 M, driven by 41% growth in Pain Management and 19% in Appendage Management; Minimally Invasive Ablation fell 34%. International sales advanced 23% (20% cc). Six-month revenue reached $259.8 M, +15.4% YoY.
Gross margin held at 74.5%. Operating loss narrowed to $6.2 M from $7.2 M; net loss improved to $6.2 M (-$0.13 EPS) vs. $8.0 M (-$0.17). YTD net loss nearly halved to $12.9 M. Cash flow from operations swung to +$10.6 M (vs. -$13.6 M). Cash & equivalents ended at $117.8 M; long-term ABL debt unchanged at $61.9 M, leaving $61.9 M in unused capacity.
R&D expense jumped 43% to $29.3 M, including a $5 M milestone for the pulsed-field ablation (PFA) Cooperation Agreement. SG&A rose 6.5% on headcount. Key milestones: FDA 510(k) clearances for AtriClip PRO-Mini and cryoICE cryoXT (launches 2H-25); completion of 6,500-patient LeAAPS stroke-prevention trial enrollment.
Risk factors: a Delaware suit from former SentreHEART holders seeks up to $260 M over PMA milestone; management deems loss not probable/estimable. Minimally invasive revenue weakness and flat margins bear monitoring.