meddevicedb.com FDA Device Reference

Dental Barrier and Sleeves

K250606 Class II Traditional
Decision Date
2025-05-29
Sponsor / Applicant
Yueying Medical Instruments (Langfang) Co., Ltd.

Technical Specification

510(k) Submission ID K250606
Product Code PEM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 2025-05-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Dental Barrier and Sleeves received FDA 510(k) clearance under submission number K250606, sponsored by Yueying Medical Instruments (Langfang) Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2025-05-29.

Classification & Regulation

This clearance is catalogued under FDA product code PEM and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.