Circadia Health, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Circadia Health, Inc. - FDA 510(k) Cleared Devices
Recent clearances: The Circadia C300 System (C300), The Circadia C300 System (C300)
2
Total
2
Cleared
0
Denied
Circadia Health, Inc. has 2 FDA 510(k) cleared medical devices. Based in El Segundo, US.
Latest FDA clearance: May 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Circadia Health, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Circadia Health, Inc.
2 devices