510(k) K211812 ยท DZE Implant, Endosseous, Root-Form
BLUEDIAMOND IMPLANT, Abutment Screw
| Applicant | Megagen Implant Co., Ltd., Daegu, KR |
| Decision | Substantially Equivalent, Jan 6, 2023 |
| Received | Jun 11, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211812
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.