510(k) K242379 ยท DZE Implant, Endosseous, Root-Form
LL Implant System
| Applicant | Ossvis Co., Ltd., Anyang-Si, KR |
| Decision | Substantially Equivalent, Nov 7, 2024 |
| Received | Aug 12, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242379
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.