K253868 is an FDA 510(k) clearance for the QuietLab Pro. This device is classified as a Device, Anti-snoring (Class II - Special Controls, product code LRK).
Submitted by QuietLab, LLC (New York, US). The FDA issued a Cleared decision on December 5, 2025, 2 days after receiving the submission on December 3, 2025.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.5570.
| 510(k) Number | K253868 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 03, 2025 |
| Decision Date | December 05, 2025 |
| Days to Decision | 2 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 |