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EzSensor Soft, EzSensor Soft i, EzSensor Bio, and EzSensor Bio i

K151707 Class II Special
Decision Date
2015-07-19
Sponsor / Applicant
Rayence Co., Ltd.

Technical Specification

510(k) Submission ID K151707
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2015-07-19
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EzSensor Soft, EzSensor Soft i, EzSensor Bio, and EzSensor Bio i received FDA 510(k) clearance under submission number K151707, sponsored by Rayence Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-07-19.

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.