Ceragroup Industries
United Statesfrom the FDA registration address FDA establishment FEI 3008501562
Ceragroup Industries is a medical device manufacturer, with 337 devices listed in FDA GUDID (FDA Class II) as of 12 Nov 2026.
- Devices
- 337
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 337
- Device classes
- FDA Class II 337
- Identifiers
- FDA FEI 3008501562
What Ceragroup Industries makes
CERAGROUP INDUSTRIES manufactures ceramic dental appliance fabrication material marketed under the name CGI, intended for use in the production of dental prosthetics and appliances.
Catalogue
Search and filter all 337 devicesShowing 1-50 of 337
Company details
- FDA FEI number
- 3008501562
- Address
- 5600 NW 12th Ave, Fort Lauderdale, FL, 33309
Frequently asked questions
How many devices does CERAGROUP INDUSTRIES have in the registry?
The registry currently lists 337 devices for CERAGROUP INDUSTRIES. Devices recorded under merged duplicate company entries are counted once.
Which registries list CERAGROUP INDUSTRIES's devices?
Among its 50 most recently registered devices, CERAGROUP INDUSTRIES has devices listed in FDA GUDID (50 devices).
What risk classes do CERAGROUP INDUSTRIES's devices fall under?
Among its 50 most recently registered devices, the classes recorded for CERAGROUP INDUSTRIES's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CERAGROUP INDUSTRIES in the registry?
The most recently registered devices listed for CERAGROUP INDUSTRIES include CGI TODA4S, CGI TSTPB, CGI TSTPBK and CGI TMODLS.