510(k) K250487 ยท NXC Aligner, Sequential
SparkTM Clear Aligner System
| Applicant | Ormco Corporation, Brea CA, US |
| Decision | Substantially Equivalent, Feb 20, 2025 |
| Received | Feb 19, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250487
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.