Continental Dental Ceramics, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3004146605
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
What Continental Dental Ceramics, Inc. makes
Continental Dental Ceramics, Inc. manufactures dental restorations, including the Luxer Shaded Zirconia—a zirconia-based ceramic material used for crowns, bridges, and other dental prosthetics.
The company’s portfolio is regulated under FDA Class II devices and listed via 510(k) premarket notifications. The manufacturer is based in the United States.
Catalogue
Cdc Zirconia Blanks Ref K122972
Regimes: 510(k) Registry: 510(k)Luxer Shaded Zirconia Ref K140070
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3004146605
- Address
- 1873 WESTERN WAY, TORRANCE, CA, 90501
Frequently asked questions
How many devices does CONTINENTAL DENTAL CERAMICS, INC. have in the registry?
The registry currently lists 2 devices for CONTINENTAL DENTAL CERAMICS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list CONTINENTAL DENTAL CERAMICS, INC.'s devices?
Among its 2 most recently registered devices, CONTINENTAL DENTAL CERAMICS, INC. has devices listed in FDA 510(k) (2 devices).
What risk classes do CONTINENTAL DENTAL CERAMICS, INC.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for CONTINENTAL DENTAL CERAMICS, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CONTINENTAL DENTAL CERAMICS, INC. in the registry?
The most recently registered devices listed for CONTINENTAL DENTAL CERAMICS, INC. include CDC ZIRCONIA BLANKS and LUXER SHADED ZIRCONIA.