510(k) K252525 ยท LRK Device, Anti-Snoring
AIO Breathe
| Applicant | Aiomega, LLC, Tyler TX, US |
| Decision | Substantially Equivalent, Nov 6, 2025 |
| Received | Aug 11, 2025 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K252525
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.