meddevicedb.com FDA Device Reference

One-Fil Putty Injectable

K251884 Class II Special
Decision Date
2025-08-22
Sponsor / Applicant
Mediclus Co., Ltd.

Technical Specification

510(k) Submission ID K251884
Product Code KIF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3820
Decision Date 2025-08-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

One-Fil Putty Injectable received FDA 510(k) clearance under submission number K251884, sponsored by Mediclus Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2025-08-22.

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.