510(k) K250353 ยท LRK Device, Anti-Snoring
Oniris; Oniris Plus
| Applicant | Oniris, Rueil Malmaison, FR |
| Decision | Substantially Equivalent, Sep 4, 2025 |
| Received | Feb 7, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250353
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.