meddevicedb.com FDA Device Reference

Non-Sterile Zirconia Block (ARENA Star, Mont Blanc)

K223253 Class II Traditional
Decision Date
2023-02-27
Sponsor / Applicant
Arum Dentistry Co., Ltd.

Technical Specification

510(k) Submission ID K223253
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2023-02-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Non-Sterile Zirconia Block (ARENA Star, Mont Blanc) received FDA 510(k) clearance under submission number K223253, sponsored by Arum Dentistry 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 2023-02-27.

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.