510(k) K261912 · LRK Device, Anti-Snoring
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| Applicant | DnB Innovations, LLC, Keller TX, US |
| Decision | Substantially Equivalent, Jul 31, 2026 |
| Received | Jun 8, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K261912
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.