Clearadvance, LLC
United Statesfrom the FDA registration address FDA FEI 3029877582
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Titan Dental Design Ref K232429
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3029877582
- DUNS number
- 119147679
- Address
- 18 Endeavor, Irvine, CA, 92618
Frequently asked questions
How many devices does Clearadvance, LLC have in the registry?
The registry currently lists 2 devices for Clearadvance, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clearadvance, LLC's devices?
Among its 2 most recently registered devices, Clearadvance, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Clearadvance, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Clearadvance, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clearadvance, LLC in the registry?
The most recently registered devices listed for Clearadvance, LLC include Titan Dental Design 1.2.7 f9 and Titan Dental Design.