meddevicedb.com FDA Device Reference

Biomic Color Opaque

K250534 Class II Traditional
Decision Date
2025-05-20
Sponsor / Applicant
Aidite (Qinhuangdao) Technology Co., Ltd.

Technical Specification

510(k) Submission ID K250534
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2025-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Biomic Color Opaque received FDA 510(k) clearance under submission number K250534, sponsored by Aidite (Qinhuangdao) 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 2025-05-20.

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.