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flag HeartBeam's cable-free, at-home 12-lead ECG device received FDA approval for remote arrhythmia detection.

flag HeartBeam, Inc. received FDA 510(k) clearance for its cable-free, at-home 12-lead ECG synthesis software, the first such device approved in the U.S. for remote arrhythmia assessment. flag The credit-card-sized device captures 3D heart signals and synthesizes them into a full ECG, which is reviewed by cardiologists. flag The approval follows a successful appeal of an earlier rejection and is backed by data showing high diagnostic accuracy. flag The company plans a limited U.S. launch in early 2026, targeting preventive cardiology practices, with future goals including heart attack detection, an extended-wear patch, and AI-powered screening tools.

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