Peerbridge Health, Inc. is one of 16378 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Peerbridge Health, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Peerbridge COR MDx (Cor MDx), Peerbridge Cor(TM) System
2
Total
2
Cleared
0
Denied
Peerbridge Health, Inc. has 2 FDA 510(k) cleared medical devices. Based in New York, US.
Latest FDA clearance: Sep 2026. Active since 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Peerbridge Health, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Peerbridge Health, Inc.
2 devices