K-number	K251626
Device name	Midmark Dental Delivery System
Applicant	Midmark Corporation
Product code	EIA
Device class	Class I
Decision date	Nov 3, 2025
Decision	Substantially Equivalent
Regulation	872.6640

AI Summary

The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →

Source

View the full FDA submission: accessdata.fda.gov

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Midmark Dental Delivery System

Everything you need for a 510(k) submission. Nothing you don't.