Data / Medical devices / United States / Ceragroup Industries
Ceragroup Industries: FDA-registered device maker in Fort Lauderdale, FL, United States, 1 510(k) clearance
Ceragroup Industries is registered with the FDA (registration 1064583) in Fort Lauderdale, FL, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 26, 2000. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 1064583
- FEI number
- 3008501562
- Address
- 5600 NW 12th Ave SUITE 304, Fort Lauderdale, FL, United States, 33309
- Owner or operator
- CERAGROUP INDUSTRIES (9040880)
- Roles
- Contract manufacturer, Manufacturer, Repackager or relabeler
- First device listed
- June 28, 2000
- Registered through
- 2027
- Brand names listed
- C-MIX, CGI, Cerakast, Ceratec, CrystalCeram
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Alloy, Metal, Base | EJH | 2 | Repackager or relabeler | accessdata.fda.gov |
| Powder, Porcelain | EIH | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Tray, Impression, Preformed | EHY | 1 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 26, 2000 | K000983 | CERAMIX PORCELAIN SYSTEM | EIH | Substantially Equivalent | C-Mix | accessdata.fda.gov |
Compare with other makers
- All makers of Powder, Porcelain
- All makers of Alloy, Metal, Base
- All makers of Tray, Impression, Preformed
Updated August 26, 2000. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.