meddevicedb.com FDA Device Reference

MULTIPLE RESIN TOOTH BONDING AGENT

K052501 Class II Traditional
Decision Date
2005-10-21
Sponsor / Applicant
Cosmedent, Inc.

Technical Specification

510(k) Submission ID K052501
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 2005-10-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTIPLE RESIN TOOTH BONDING AGENT received FDA 510(k) clearance under submission number K052501, sponsored by Cosmedent, 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 2005-10-21.

Classification & Regulation

This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.