meddevicedb.com FDA Device Reference

Calcium Hydroxide Temporary Filling Material (KP-Cal)

K261514 Class II Traditional
Decision Date
2026-08-25
Sponsor / Applicant
Guilin Kevin Peter Technology Co., Ltd.

Technical Specification

510(k) Submission ID K261514
Product Code KIF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3820
Decision Date 2026-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Calcium Hydroxide Temporary Filling Material (KP-Cal) received FDA 510(k) clearance under submission number K261514, sponsored by Guilin Kevin Peter Technology 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 2026-08-25.

Classification & Regulation

This clearance is catalogued under FDA product code KIF and 21 CFR 872.3820, within the Dental review panel as a Class II device.