510(k) K210203 ยท LRK Device, Anti-Snoring
mmRNA appliance
| Applicant | Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I), Highland Ranch CO, US |
| Decision | Substantially Equivalent, Aug 19, 2021 |
| Received | Jan 26, 2021 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K210203
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.