510(k) K232151 · NHA Abutment, Implant, Dental, Endosseous
Dynamic TiBase
| Applicant | Talladium España, SL, Lleida, ES |
| Decision | Substantially Equivalent, Oct 17, 2023 |
| Received | Jul 19, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232151
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.