510(k) K250343 ยท NXC Aligner, Sequential
LuxCreo Clear Aligner System
| Applicant | LuxCreo, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Apr 8, 2025 |
| Received | Feb 6, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K250343
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.