Zbeats, Inc. is one of 16407 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zbeats, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ZBPro Diagnostic (Version 2.0), ZBPro Diagnostic
2
Total
2
Cleared
0
Denied
Zbeats, Inc. has 2 FDA 510(k) cleared medical devices. Based in Stony Brook, US.
Latest FDA clearance: Sep 2026. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Zbeats, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Zaliance Medical Solutions and Zaliance Medical Solutions, LLC.
FDA 510(k) Regulatory Record - Zbeats, Inc.
2 devices