meddevicedb.com FDA Device Reference

Mei Ceramic Bracket

K190608 Class II Traditional
Decision Date
2019-11-04
Sponsor / Applicant
Orthosun Co., Ltd.

Technical Specification

510(k) Submission ID K190608
Product Code NJM
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 2019-11-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Mei Ceramic Bracket received FDA 510(k) clearance under submission number K190608, sponsored by Orthosun 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 2019-11-04.

Classification & Regulation

This clearance is catalogued under FDA product code NJM and 21 CFR 872.5470, within the Dental review panel as a Class II device.