K253683 is an FDA 510(k) clearance for the FAQ? (LED Panel); FAQ? (Dual LED Panel), a Light Based Over The Counter Wrinkle Reduction (Class II — Special Controls, product code OHS), submitted by Foreo, Inc. (Las Vegas, US). The FDA issued a Cleared decision on February 20, 2026, 91 days after receiving the submission on November 21, 2025. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4810.
| 510(k) Number | K253683 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 21, 2025 |
| Decision Date | February 20, 2026 |
| Days to Decision | 91 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Statement |
| Product Code | OHS — Light Based Over The Counter Wrinkle Reduction |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.4810 |
| Definition | Use Of Light Based Treatment To Reduce Wrinkles On The Body In General Or Specific Anatomical Locations Depending On The Information Provided. |