meddevicedb.com FDA Device Reference

Ultrasound Therapy Workstation (XMS-UET2)

K244041 Class II Traditional
Decision Date
2025-10-07
Sponsor / Applicant
Xemis Medical Technology (Shenzhen) Co., Ltd.

Technical Specification

510(k) Submission ID K244041
Product Code IMG
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5860
Decision Date 2025-10-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Ultrasound Therapy Workstation (XMS-UET2) received FDA 510(k) clearance under submission number K244041, sponsored by Xemis Medical Technology (Shenzhen) Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2025-10-07.

Classification & Regulation

This clearance is catalogued under FDA product code IMG and 21 CFR 890.5860, within the Physical Medicine review panel as a Class II device.