meddevicedb.com FDA Device Reference

Any-Cem

K254201 Class II Traditional
Decision Date
2026-08-13
Sponsor / Applicant
Mediclus Co., Ltd.

Technical Specification

510(k) Submission ID K254201
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 2026-08-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Any-Cem received FDA 510(k) clearance under submission number K254201, sponsored by Mediclus 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 2026-08-13.

Classification & Regulation

This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.