510(k) K261251 · LRK Device, Anti-Snoring
Snorbliss® Anti-Snoring Device
| Applicant | Endeavor Commerce, LLC, Sheridan WY, US |
| Decision | Substantially Equivalent, Jun 11, 2026 |
| Received | Apr 16, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K261251
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.