meddevicedb.com FDA Device Reference

Resin for Temporary Crown & Bridge

K180657 Class II Traditional
Decision Date
2018-12-07
Sponsor / Applicant
Dentis Co., Ltd.

Technical Specification

510(k) Submission ID K180657
Product Code EBG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3770
Decision Date 2018-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Resin for Temporary Crown & Bridge received FDA 510(k) clearance under submission number K180657, sponsored by Dentis 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 2018-12-07.

Classification & Regulation

This clearance is catalogued under FDA product code EBG and 21 CFR 872.3770, within the Dental review panel as a Class II device.