meddevicedb.com FDA Device Reference

Oral Surgery System and Accessories

K152125 Class II Traditional
Decision Date
2016-08-15
Sponsor / Applicant
Bonart Co., Ltd.

Technical Specification

510(k) Submission ID K152125
Product Code DZI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4120
Decision Date 2016-08-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Oral Surgery System and Accessories received FDA 510(k) clearance under submission number K152125, sponsored by Bonart Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2016-08-15.

Classification & Regulation

This clearance is catalogued under FDA product code DZI and 21 CFR 872.4120, within the Dental review panel as a Class II device.