meddevicedb.com FDA Device Reference

Non-Sterile Zirconia Block

K190112 Class II Traditional
Decision Date
2019-12-20
Sponsor / Applicant
Fine Advanced Compound Co., Ltd.

Technical Specification

510(k) Submission ID K190112
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2019-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Non-Sterile Zirconia Block received FDA 510(k) clearance under submission number K190112, sponsored by Fine Advanced Compound 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 2019-12-20.

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.