510(k) K262937 ยท LRK Device, Anti-Snoring
PDR Airway Device
| Applicant | Park Dental Research Corp., Ardmore OK, US |
| Decision | Substantially Equivalent, Oct 20, 2026 |
| Received | Aug 21, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K262937
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.