meddevicedb.com FDA Device Reference

Dental Zirconia Block (Models HT-plus, ST, SHT, UT, 3D-Pro)

K240912 Class II Traditional
Decision Date
2024-05-31
Sponsor / Applicant
Anhui Miisen Intelligence Technology Co., Ltd.

Technical Specification

510(k) Submission ID K240912
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2024-05-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Dental Zirconia Block (Models HT-plus, ST, SHT, UT, 3D-Pro) received FDA 510(k) clearance under submission number K240912, sponsored by Anhui Miisen Intelligence Technology 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 2024-05-31.

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.