Heartbeam (BEAT) Registration Filing summary
Event summary combining transcript, slides, and related documents.
Registration Filing summary
9 Feb, 2026Company overview and business model
Focuses on ambulatory cardiac monitoring with a proprietary 3D ECG platform enabling cable-free, high-fidelity 12-lead ECG readings outside healthcare facilities.
Initial product, HeartBeam System, is FDA-cleared for arrhythmia assessment and features a portable, credit card-sized device, patient app, physician portal, and cloud-based algorithms.
Growth strategy includes limited launch in early 2026, expansion into heart attack detection, development of an extended wear patch, and leveraging AI for predictive analytics.
Holds 24 issued patents worldwide, with additional pending applications, supporting future product expansion into patches and smartwatch-based monitors.
Targets concierge and preventive cardiology groups, with plans to expand to broader markets and partner with payors for reimbursement.
Financial performance and metrics
As of December 31, 2025, had 40,117,404 shares of common stock outstanding and no preferred stock issued.
16 employees as of year-end 2025, increasing to 17 in January 2026 with the hiring of a Chief Commercial Officer.
$78.8 million of previously registered securities remain unsold and are included in the current registration.
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 portable ECG system targets $100M capital raise in expanding cardiac monitoring market.BEAT
Registration Filing13 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 - 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