510(k) K251628 ยท LRK Device, Anti-Snoring
Mandibular Advancement Device L07
| Applicant | Dcstar, Inc., New York NY, US |
| Decision | Substantially Equivalent, Oct 22, 2025 |
| Received | May 28, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251628
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.