meddevicedb.com FDA Device Reference

Dental Impression Material

K211489 Class II Traditional
Decision Date
2021-07-28
Sponsor / Applicant
Nanchang Dental Bright Technology Co., Ltd.

Technical Specification

510(k) Submission ID K211489
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 2021-07-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Dental Impression Material received FDA 510(k) clearance under submission number K211489, sponsored by Nanchang Dental Bright 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 2021-07-28.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.