Carbon, Inc.
United Statesfrom the FDA registration address FDA FEI 3046274075
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
DB 4000 High Impact Denture Base Ref K260569
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3046274075
- Address
- 1272 Borregas Ave, Sunnyvale, CA, 94089
Frequently asked questions
How many devices does Carbon, Inc. have in the registry?
The registry currently lists 1 device for Carbon, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Carbon, Inc.'s devices?
Among its 1 most recently registered device, Carbon, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Carbon, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Carbon, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Carbon, Inc. in the registry?
The most recently registered devices listed for Carbon, Inc. include DB 4000 High Impact Denture Base.