GoldenDent
United Statesfrom the FDA registration address FDA FEI 3005972890
- Devices
- 147
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 147 devicesShowing 1-50 of 147
Company details
- FDA FEI number
- 3005972890
- DUNS number
- 078273228
- Address
- 27251 Gratiot Ave, Roseville, MI, 48066
Frequently asked questions
How many devices does GoldenDent have in the registry?
The registry currently lists 147 devices for GoldenDent. Devices recorded under merged duplicate company entries are counted once.
Which registries list GoldenDent's devices?
Among its 50 most recently registered devices, GoldenDent has devices listed in FDA GUDID (50 devices).
What risk classes do GoldenDent's devices fall under?
Among its 50 most recently registered devices, the classes recorded for GoldenDent's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from GoldenDent in the registry?
The most recently registered devices listed for GoldenDent include GoldenDent GTS2-31, GoldenDent GTAK-21, GoldenDent GH IK and GoldenDent SPGA3.