Heartbeam (BEAT) Registration Filing summary
Event summary combining transcript, slides, and related documents.
Registration Filing summary
13 Mar, 2026Company overview and business model
Focuses on ambulatory cardiac monitoring with a proprietary 3D ECG platform enabling synthesized 12-lead ECGs outside healthcare facilities.
Initial product is an FDA-cleared, cable-free, credit card-sized ECG device with cloud-based algorithms and a physician portal.
Targets high-risk coronary artery disease monitoring, arrhythmia assessment, and future heart attack detection.
Growth strategy includes limited launch in 2026, expansion into heart attack detection, extended wear patch, and AI-based diagnostics.
Employs 17 staff as of January 2026, with commercialization led by an experienced Chief Commercial Officer.
Financial performance and metrics
As of March 11, 2026, 41,087,871 shares of common stock are outstanding, held by approximately 45 shareholders.
Common stock last traded at $1.47 per share on March 12, 2026, on Nasdaq Capital Market.
Financial statements for 2024 and 2025 audited by independent firms, both including going concern explanatory paragraphs.
Use of proceeds and capital allocation
Net proceeds from securities sales will be used as set forth in the applicable prospectus supplement.
Latest events from Heartbeam
- At-home 12-lead ECG platform launches with subscription model and AI-driven expansion.BEAT
Oppenheimer 36th Annual Healthcare MedTech & Services Conference16 Mar 2026 - FDA-cleared 12-lead ECG launch, AI partnership, and improved cash position drive growth.BEAT
Q4 202512 Mar 2026 - FDA-cleared, cable-free 12-lead ECG platform targets $40B+ cardiac monitoring market.BEAT
Investor presentation12 Mar 2026 - Shelf registration for $100M supports launch of FDA-cleared portable 12-lead ECG system.BEAT
Registration Filing9 Feb 2026 - Q3 net loss was $5.3M; FDA clearance and commercial launch expected by end of 2025.BEAT
Q3 20253 Feb 2026 - AIMIGO nears FDA clearance as Q2 net loss hits $5M and cash burn raises going concern risk.BEAT
Q2 20241 Feb 2026 - Q3 net loss reached $5.0M; FDA clearance and new funding are critical for future operations.BEAT
Q3 202415 Jan 2026 - FDA clearance and $11.5M funding drive commercial launch of cardiac monitoring technology.BEAT
Q4 202425 Dec 2025 - Annual meeting to elect directors, ratify auditor, and expand equity plan for long-term growth.BEAT
Proxy Filing2 Dec 2025