510(k) K230108 · DZE Implant, Endosseous, Root-Form
Straumann® BLC and TLC Implants
| Applicant | Institut Straumann AG, Basel, CH |
| Decision | Substantially Equivalent, Sep 14, 2023 |
| Received | Jan 13, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230108
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.