meddevicedb.com FDA Device Reference

TrusFIL-Flow Flowable Composite Restorative

K221510 Class II Traditional
Decision Date
2022-10-12
Sponsor / Applicant
Rizhao Huge Biomaterials Company, Ltd.

Technical Specification

510(k) Submission ID K221510
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2022-10-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TrusFIL-Flow Flowable Composite Restorative received FDA 510(k) clearance under submission number K221510, sponsored by Rizhao Huge Biomaterials Company, 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 2022-10-12.

Classification & Regulation

This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.