K250687 is an FDA 510(k) clearance for the Cocoon Solo (DX-7020s). This device is classified as a System, X-ray, Extraoral Source, Digital (Class II - Special Controls, product code MUH).
Submitted by Dexcowin Global, Inc. (Pasadena, US). The FDA issued a Cleared decision on October 24, 2025, 232 days after receiving the submission on March 6, 2025.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 872.1800.
| 510(k) Number | K250687 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 06, 2025 |
| Decision Date | October 24, 2025 |
| Days to Decision | 232 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | MUH - System, X-ray, Extraoral Source, Digital |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.1800 |