meddevicedb.com FDA Device Reference

BioHorizons CEREC Compatible Ti-Bases

K260061 Class II Traditional
Decision Date
2026-06-26
Sponsor / Applicant
BioHorizons Implant Systems, Inc.

Technical Specification

510(k) Submission ID K260061
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2026-06-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BioHorizons CEREC Compatible Ti-Bases received FDA 510(k) clearance under submission number K260061, sponsored by BioHorizons Implant Systems, 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 2026-06-26.

Classification & Regulation

This clearance is catalogued under FDA product code NHA and 21 CFR 872.3630, within the Dental review panel as a Class II device.