Encore Laboratory
Country not established FDA establishment FEI 3020749939
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- GUDID
- GUDID
- GUDID
- GUDID
Company details
- FDA FEI number
- 3020749939
- Address
- 1520 BROOKHOLLOW DR, Santa Ana, CA, 92705
Frequently asked questions
How many devices does ENCORE LABORATORY have in the registry?
The registry currently lists 4 devices for ENCORE LABORATORY. Devices recorded under merged duplicate company entries are counted once.
Which registries list ENCORE LABORATORY's devices?
Among its 4 most recently registered devices, ENCORE LABORATORY has devices listed in FDA GUDID (4 devices).
What risk classes do ENCORE LABORATORY's devices fall under?
Among its 4 most recently registered devices, the classes recorded for ENCORE LABORATORY's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ENCORE LABORATORY in the registry?
The most recently registered devices listed for ENCORE LABORATORY include enCore Night Guard Hybrid, enCore Night Guard Hard, enCore Night Guard Soft and enCore Night Guard Putty - OTC.