Upcera Dental America Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3019596325
- Devices
- 40
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Search and filter all 40 devicesCompany details
- FDA FEI number
- 3019596325
- Address
- 13100 Alondra Blvd. Ste. 105, Cerritos, CA, 90703
Frequently asked questions
How many devices does UPCERA DENTAL AMERICA INC. have in the registry?
The registry currently lists 40 devices for UPCERA DENTAL AMERICA INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list UPCERA DENTAL AMERICA INC.'s devices?
Among its 40 most recently registered devices, UPCERA DENTAL AMERICA INC. has devices listed in FDA GUDID (40 devices).
What risk classes do UPCERA DENTAL AMERICA INC.'s devices fall under?
Among its 40 most recently registered devices, the classes recorded for UPCERA DENTAL AMERICA INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from UPCERA DENTAL AMERICA INC. in the registry?
The most recently registered devices listed for UPCERA DENTAL AMERICA INC. include Artouch E-Str D A2, Artouch E-Str T Blue, Artouch E-Str SM Sunny Beach and Artouch E-Str M Cream.