meddevicedb.com FDA Device Reference

EzSensor HD, EzSensor UHD

K252570 Class II Special
Decision Date
2025-11-10
Sponsor / Applicant
Qpix Solutions, Inc.

Technical Specification

510(k) Submission ID K252570
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2025-11-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EzSensor HD, EzSensor UHD received FDA 510(k) clearance under submission number K252570, sponsored by Qpix Solutions, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2025-11-10.

Classification & Regulation

This clearance is catalogued under FDA product code MUH and 21 CFR 872.1800, within the Dental review panel as a Class II device.