meddevicedb.com FDA Device Reference

Cemented Plus Abutment

K262207 Class II Traditional
Decision Date
2026-09-23
Sponsor / Applicant
Unidental Co., Ltd.

Technical Specification

510(k) Submission ID K262207
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2026-09-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Cemented Plus Abutment received FDA 510(k) clearance under submission number K262207, sponsored by Unidental Co., 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 2026-09-23.

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.