Apex Dental Sleep Lab
United Statesfrom the FDA registration address FDA establishment FEI 3012716038
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3012716038
- Address
- 7863 La Mesa, La Mesa, CA, 91942
Frequently asked questions
How many devices does APEX DENTAL SLEEP LAB have in the registry?
The registry currently lists 5 devices for APEX DENTAL SLEEP LAB. Devices recorded under merged duplicate company entries are counted once.
Which registries list APEX DENTAL SLEEP LAB's devices?
Among its 5 most recently registered devices, APEX DENTAL SLEEP LAB has devices listed in FDA GUDID (5 devices).
What risk classes do APEX DENTAL SLEEP LAB's devices fall under?
Among its 5 most recently registered devices, the classes recorded for APEX DENTAL SLEEP LAB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from APEX DENTAL SLEEP LAB in the registry?
The most recently registered devices listed for APEX DENTAL SLEEP LAB include KAVA DORSAL ACRYLIC LQZ, KAVA HERBST ACRYLIC LQZ, KAVA DORSAL DUAL LAMINATE LQZ and KAVA HERBST 3D LQZ.