meddevicedb.com FDA Device Reference

ENDO-EXPRESS (R) HANDPIECE

K111541 Class I Traditional
Decision Date
2012-03-16
Sponsor / Applicant
Essential Dental Systems, Inc.

Technical Specification

510(k) Submission ID K111541
Product Code EGS
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 2012-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDO-EXPRESS (R) HANDPIECE received FDA 510(k) clearance under submission number K111541, sponsored by Essential Dental Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2012-03-16.

Classification & Regulation

This clearance is catalogued under FDA product code EGS and 21 CFR 872.4200, within the Dental review panel as a Class I device.