meddevicedb.com FDA Device Reference

Zirconia Block

K241316 Class II Traditional
Decision Date
2024-07-09
Sponsor / Applicant
Hunan Hualian Special Ceramics Co., Ltd.

Technical Specification

510(k) Submission ID K241316
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2024-07-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Zirconia Block received FDA 510(k) clearance under submission number K241316, sponsored by Hunan Hualian Special Ceramics 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 2024-07-09.

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.