510(k) K220390 ยท NHA Abutment, Implant, Dental, Endosseous
CreoDent Solidex Customized Abutment and Screw
| Applicant | Creodent Prosthetics, Ltd., New York NY, US |
| Decision | Substantially Equivalent, Dec 2, 2022 |
| Received | Feb 11, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220390
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.