510(k) K211427 ยท NXC Aligner, Sequential
CREOKORREKT Aligners
| Applicant | Creodent Prosthetics, Ltd., New York NY, US |
| Decision | Substantially Equivalent, Oct 13, 2022 |
| Received | May 7, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211427
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.