meddevicedb.com FDA Device Reference

NanoCeram Resin

K262681 Class II Traditional
Decision Date
2026-07-31
Sponsor / Applicant
3BFAB TEKNOLOJI A.S.

Technical Specification

510(k) Submission ID K262681
Product Code EBI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3760
Decision Date 2026-07-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NanoCeram Resin received FDA 510(k) clearance under submission number K262681, sponsored by 3BFAB TEKNOLOJI A.S.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2026-07-31.

Classification & Regulation

This clearance is catalogued under FDA product code EBI and 21 CFR 872.3760, within the Dental review panel as a Class II device.