K231138 is an FDA 510(k) clearance for the Aniti-Snore Mouthguard+. This device is classified as a Device, Anti-snoring (Class II - Special Controls, product code LRK).
Submitted by Oscimed SA (Suisse, CH). The FDA issued a Cleared decision on January 16, 2024, 270 days after receiving the submission on April 21, 2023.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.5570.
| 510(k) Number | K231138 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 21, 2023 |
| Decision Date | January 16, 2024 |
| Days to Decision | 270 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | LRK - Device, Anti-snoring |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.5570 |