Gergens Orthodontic Lab
United Statesfrom the FDA registration address FDA establishment FEI 3008274496
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Acrylic Herbst Appliance with Micro-Recorder Ref K170606
Regimes: 510(k) Registry: 510(k)Dorsal Appliance Ref K143591
Regimes: 510(k) Registry: 510(k)Acrylic Herbst Appliance Ref K113126
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3008274496
- Address
- 1745 West Deer Valley Rd, Phoenix, AZ, 85027
Frequently asked questions
How many devices does GERGENS ORTHODONTIC LAB have in the registry?
The registry currently lists 3 devices for GERGENS ORTHODONTIC LAB. Devices recorded under merged duplicate company entries are counted once.
Which registries list GERGENS ORTHODONTIC LAB's devices?
Among its 3 most recently registered devices, GERGENS ORTHODONTIC LAB has devices listed in FDA 510(k) (3 devices).
What risk classes do GERGENS ORTHODONTIC LAB's devices fall under?
Among its 3 most recently registered devices, the classes recorded for GERGENS ORTHODONTIC LAB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from GERGENS ORTHODONTIC LAB in the registry?
The most recently registered devices listed for GERGENS ORTHODONTIC LAB include Acrylic Herbst Appliance with Micro-Recorder, Dorsal Appliance and ACRYLIC HERBST APPLIANCE.