Circadia Health, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3017812398
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
The Circadia CX00 System (CX00) Ref K262447
Regimes: 510(k) Registry: 510(k)The Circadia C300 System (C300) Ref K261286
Regimes: 510(k) Registry: 510(k)The Circadia C300 System (C300) Ref K252676
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3017812398
- Address
- 507 S Douglas St, El Segundo, CA, 90245
Frequently asked questions
How many devices does Circadia Health, Inc. have in the registry?
The registry currently lists 3 devices for Circadia Health, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Circadia Health, Inc.'s devices?
Among its 3 most recently registered devices, Circadia Health, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Circadia Health, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Circadia Health, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Circadia Health, Inc. in the registry?
The most recently registered devices listed for Circadia Health, Inc. include The Circadia CX00 System (CX00) and The Circadia C300 System (C300).