meddevicedb.com FDA Device Reference

Dental Zirconia Ceramic

K213570 Class II Traditional
Decision Date
2022-01-07
Sponsor / Applicant
Aidite (Qinhuangdao) Technology Co., Ltd.

Technical Specification

510(k) Submission ID K213570
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2022-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Dental Zirconia Ceramic received FDA 510(k) clearance under submission number K213570, sponsored by Aidite (Qinhuangdao) Technology 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 2022-01-07.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.