510(k) K220140 ยท NXC Aligner, Sequential
ClearCorrect System
| Applicant | Clearcorrect, LLC, Round Rock TX, US |
| Decision | Substantially Equivalent, Oct 5, 2022 |
| Received | Jan 18, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220140
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.