meddevicedb.com FDA Device Reference

APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste)

K260830 Class II Traditional
Decision Date
2026-03-18
Sponsor / Applicant
Sangi Co., Ltd.

Technical Specification

510(k) Submission ID K260830
Product Code LBH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3260
Decision Date 2026-03-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste) received FDA 510(k) clearance under submission number K260830, sponsored by Sangi 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 2026-03-18.

Classification & Regulation

This clearance is catalogued under FDA product code LBH and 21 CFR 872.3260, within the Dental review panel as a Class II device.