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ZBeats Receives FDA Clearance for ZBPro Diagnostic v2.0, Supporting ECG Analysis Up to 14 DaysExpanded platform supports wearable patches across diverse recording devices; Company to showcase new capabilities at HRX 2026 in Atlanta. STONY BROOK, N.Y., Sept. 15, 2026 /PRNewswire/ -- ZBeats Inc. today announced it has received U.S. Food and Drug Administration (FDA) 510(k) clearance (K261580) for its ZBPro Diagnostic v2.0 software. This clearance expands ZBeats' independent ECG analysis platform to support recordings from one minute up to 14 days, including Holter configurations and wearable patches. The ZBeats team will showcase the newly cleared version this week at HRX Live 2026 in Atlanta, Georgia.
FDA clears ZBPro Diagnostic v2.0, advancing independent ECG intelligence across wearable and clinical workflows. Experience ZBPro v2.0 at HRX 2026 "This clearance advances our vision for independent ECG intelligence," said Bin Fang, PhD, CEO and co-founder of ZBeats, Inc. "ZBPro combines NoiseGuard with a common intelligence layer that transforms data from supported recording technologies into consistent, clinically meaningful analysis at scale. By separating ECG intelligence from the hardware, ZBPro creates a flexible foundation for clinical research, monitoring centers, and consumer wearables." ZBPro combines automated retrospective beat and rhythm analysis, including detection of atrial fibrillation, with advanced review, editing, and reporting tools in an intuitive technician interface. Flexible workflows and configurable permissions help clinical teams standardize review and move studies efficiently from analysis to final report, improving operational efficiency for high-volume IDTFs. About ZBeats Inc.
SOURCE ZBeats Inc.
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