510(k) K230104 · DZE Implant, Endosseous, Root-Form
Anthogyr AXIOM® BL X3 implants, Anthogyr Multi-Unit components for AXIOM® BL
| Applicant | Anthogyr, Sallanches, FR |
| Decision | Substantially Equivalent, Oct 16, 2023 |
| Received | Jan 13, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230104
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.