510(k) K223339 ยท DZE Implant, Endosseous, Root-Form
Bone Chamber Implant
| Applicant | Megagen Implant Co., Ltd., Daegu, KR |
| Decision | Substantially Equivalent, Jul 18, 2023 |
| Received | Nov 1, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223339
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.