Phoenix Orthodontics Inc
United Statesfrom the FDA registration address FDA establishment FEI 3009491780
- Devices
- 785
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Search and filter all 785 devicesShowing 1-50 of 785
Company details
- FDA FEI number
- 3009491780
- Address
- 3750 Palladian Village Drive, Marietta, GA, 30066
Frequently asked questions
How many devices does Phoenix Orthodontics Inc have in the registry?
The registry currently lists 785 devices for Phoenix Orthodontics Inc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Phoenix Orthodontics Inc's devices?
Among its 50 most recently registered devices, Phoenix Orthodontics Inc has devices listed in FDA GUDID (50 devices).
What risk classes do Phoenix Orthodontics Inc's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Phoenix Orthodontics Inc's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Phoenix Orthodontics Inc in the registry?
The most recently registered devices listed for Phoenix Orthodontics Inc include Phoenix Elastics E-450-BC, Phoenix Nickel Titanium N-SYM-016U, Phoenix Ultra Mini Tie E-T-UMCB and Phoenix Nickel Titanium N-TIPU-2020.