meddevicedb.com FDA Device Reference

Dental Barriers and Sleeves (AB0006)

K261956 Class II Traditional
Decision Date
2026-09-08
Sponsor / Applicant
ANI Co., Ltd.

Technical Specification

510(k) Submission ID K261956
Product Code PEM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 2026-09-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Dental Barriers and Sleeves (AB0006) received FDA 510(k) clearance under submission number K261956, sponsored by ANI 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 2026-09-08.

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.