510(k) K250739 ยท NXC Aligner, Sequential
Primeprint Direct Aligner
| Applicant | Dreve Dentamid GmbH, Unna, DE |
| Decision | Substantially Equivalent, Nov 7, 2025 |
| Received | Mar 11, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250739
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.