# Circadia Health, Inc.

- Location (FDA's records): El Segundo, CA
- FDA decisions: 3 (2026–2026): 3 510(k) clearances
- Product codes: DRT (3)
- 510(k) review time since 2016: median 91 days, against 120 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Circadia Technologies, Ltd.: 1 (https://510kreport.com/company/circadia-technologies)

## Its most-cited devices
- K252676: The Circadia C300 System (C300) (2026), cited by 1

## Recent decisions
- K262447: The Circadia CX00 System (CX00) (Oct 15, 2026)
- K261286: The Circadia C300 System (C300) (May 20, 2026)
- K252676: The Circadia C300 System (C300) (Feb 3, 2026)

Source page: https://510kreport.com/company/circadia-health