Brevet Inc.
United Statesfrom the FDA registration address FDA establishment FEI 2025870
- Devices
- 6
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Brevet Cassette Sterilization Module Ref K882617
Regimes: 510(k) Registry: 510(k)Brevet Floss Pick (Autoclave Sterilizer) Ref K895958
Regimes: 510(k) Registry: 510(k)Brevet Disposable Connectors Ref K895753
Regimes: 510(k) Registry: 510(k)Brevet Floss Pick (Cold Sterilization Fluids) Ref K895959
Regimes: 510(k) Registry: 510(k)Small Instrument Sterilization/Bur Box Ref K910794
Regimes: 510(k) Registry: 510(k)Brevet Dental Instruments Ref K883126
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 2025870
- Address
- 21571 Surveyor Circle, Huntington Beach, CA, 92646
Frequently asked questions
How many devices does BREVET INC. have in the registry?
The registry currently lists 6 devices for BREVET INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list BREVET INC.'s devices?
Among its 6 most recently registered devices, BREVET INC. has devices listed in FDA 510(k) (6 devices).
What risk classes do BREVET INC.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for BREVET INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from BREVET INC. in the registry?
The most recently registered devices listed for BREVET INC. include BREVET CASSETTE STERILIZATION MODULE, BREVET FLOSS PICK (AUTOCLAVE STERILIZER), BREVET DISPOSABLE CONNECTORS and BREVET FLOSS PICK (COLD STERILIZATION FLUIDS).