meddevicedb.com FDA Device Reference

Bond-PR™ Universal Adhesive

K260682 Class II Traditional
Decision Date
2026-03-03
Sponsor / Applicant
Premier Dental Products Company

Technical Specification

510(k) Submission ID K260682
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 2026-03-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Bond-PR™ Universal Adhesive received FDA 510(k) clearance under submission number K260682, sponsored by Premier Dental Products Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2026-03-03.

Classification & Regulation

This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.