meddevicedb.com FDA Device Reference

Transcend Bulk Fill Flowable Composite

K262228 Class II Traditional
Decision Date
2026-07-01
Sponsor / Applicant
Ultradent Products, Inc.

Technical Specification

510(k) Submission ID K262228
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2026-07-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Transcend Bulk Fill Flowable Composite received FDA 510(k) clearance under submission number K262228, sponsored by Ultradent Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2026-07-01.

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.