meddevicedb.com FDA Device Reference

ARENA Star, Galaxy Star

K250063 Class II Traditional
Decision Date
2025-07-10
Sponsor / Applicant
Arum Dentistry Co., Ltd.

Technical Specification

510(k) Submission ID K250063
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2025-07-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARENA Star, Galaxy Star received FDA 510(k) clearance under submission number K250063, sponsored by Arum Dentistry 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 2025-07-10.

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.