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TOKUYAMA BOND FORCE

K070215 Class II Traditional
Decision Date
2007-03-30
Sponsor / Applicant
Tokuyama Dental Corporation

Technical Specification

510(k) Submission ID K070215
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 2007-03-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOKUYAMA BOND FORCE received FDA 510(k) clearance under submission number K070215, sponsored by Tokuyama Dental Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2007-03-30.

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.