510(k) K212533 · DZE Implant, Endosseous, Root-Form
BLX WB Ø5.0 (L18), Ø5.5 and Ø6.5 mm (L14 and L16) Implants
| Applicant | Institut Straumann AG, Basel, CH |
| Decision | Substantially Equivalent, Jan 28, 2022 |
| Received | Aug 11, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212533
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.