510(k) K190394 ยท NXC Aligner, Sequential
SunClear Aligner system
| Applicant | Sun Dental Laboratories, LLC, St. Petersburg FL, US |
| Decision | Substantially Equivalent, Dec 16, 2019 |
| Received | Feb 19, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190394
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.