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Tuxedo Digital Dental Sensor

K153710 Class II Traditional
Decision Date
2016-03-18
Sponsor / Applicant
Led Dental, Inc.

Technical Specification

510(k) Submission ID K153710
Product Code MQB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 2016-03-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Tuxedo Digital Dental Sensor received FDA 510(k) clearance under submission number K153710, sponsored by Led Dental, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2016-03-18.

Classification & Regulation

This clearance is catalogued under FDA product code MQB and 21 CFR 892.1680, within the Radiology review panel as a Class II device.