K251626 is an FDA 510(k) clearance for the Midmark Dental Delivery System. This device is classified as a Unit, Operative Dental (Class I - General Controls, product code EIA).
Submitted by Midmark Corporation (Versailles, US). The FDA issued a Cleared decision on November 3, 2025, 159 days after receiving the submission on May 28, 2025.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.6640.
| 510(k) Number | K251626 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 28, 2025 |
| Decision Date | November 03, 2025 |
| Days to Decision | 159 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | EIA - Unit, Operative Dental |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 872.6640 |