510(k) K231387 ยท KIF Resin, Root Canal Filling
Endofill
| Applicant | Lumendo AG, Renens, CH |
| Decision | Substantially Equivalent, Jul 10, 2023 |
| Received | May 12, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231387
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.