meddevicedb.com FDA Device Reference

Midmark Dental Delivery System

K251626 Class I Traditional
Decision Date
2025-11-03
Sponsor / Applicant
Midmark Corporation

Technical Specification

510(k) Submission ID K251626
Product Code EIA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6640
Decision Date 2025-11-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Midmark Dental Delivery System received FDA 510(k) clearance under submission number K251626, sponsored by Midmark Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2025-11-03.

Classification & Regulation

This clearance is catalogued under FDA product code EIA and 21 CFR 872.6640, within the Dental review panel as a Class I device.