meddevicedb.com FDA Device Reference

Any-Com Bulk

K242713 Class II Traditional
Decision Date
2025-02-07
Sponsor / Applicant
Mediclus Co., Ltd.

Technical Specification

510(k) Submission ID K242713
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2025-02-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Any-Com Bulk received FDA 510(k) clearance under submission number K242713, 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 2025-02-07.

Classification & Regulation

This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.