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Dual Cure Resin Cement

K201790 Class II Traditional
Decision Date
2020-09-29
Sponsor / Applicant
Rizhao Huge Biomaterials Company, Ltd.

Technical Specification

510(k) Submission ID K201790
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 2020-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Dual Cure Resin Cement received FDA 510(k) clearance under submission number K201790, sponsored by Rizhao Huge Biomaterials Company, 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 2020-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.