K252120 is an FDA 510(k) clearance for the Fundus On Phone Non Mydriatic (FOP NM-10). This device is classified as a Camera, Ophthalmic, Ac-powered (Class II - Special Controls, product code HKI).
Submitted by Remidio Innovative Solutions Private Limited (Bengaluru, IN). The FDA issued a Cleared decision on December 12, 2025, 158 days after receiving the submission on July 7, 2025.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.1120.
| 510(k) Number | K252120 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 07, 2025 |
| Decision Date | December 12, 2025 |
| Days to Decision | 158 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Summary PDF |
| Product Code | HKI - Camera, Ophthalmic, Ac-powered |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 886.1120 |