510(k) K253355 ยท LRK Device, Anti-Snoring
Difiney Advanced Anti Snoring Device 4.0
| Applicant | Fissiontech, LLC, New York NY, US |
| Decision | Substantially Equivalent, Oct 29, 2025 |
| Received | Sep 30, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K253355
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.