510(k) K242929 ยท NXC Aligner, Sequential
Fas Aligner System
| Applicant | Xplora 3D Europe S.L, Madrid, ES |
| Decision | Substantially Equivalent, Dec 20, 2024 |
| Received | Sep 24, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242929
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.