510(k) K212680 ยท NXC Aligner, Sequential
LuxCreo Clear Aligner System
| Applicant | LuxCreo, Inc., Belmont CA, US |
| Decision | Substantially Equivalent, May 31, 2022 |
| Received | Aug 24, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212680
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.