510(k) K223113 ยท NHA Abutment, Implant, Dental, Endosseous
Medentika Abutment System, Medentika CAD/CAM Abutments, Medentika CAD/CAM TiBases, Medentika Multi-unit Abutments
| Applicant | Medentika GmbH, Hugelsheim, DE |
| Decision | Substantially Equivalent, Apr 15, 2024 |
| Received | Oct 3, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223113
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.