meddevicedb.com FDA Device Reference

Elos Accurate® Denture Fixation System

K253774 Class II Traditional
Decision Date
2026-05-20
Sponsor / Applicant
Elos Medtech Pinol A/S

Technical Specification

510(k) Submission ID K253774
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2026-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Elos Accurate® Denture Fixation System received FDA 510(k) clearance under submission number K253774, sponsored by Elos Medtech Pinol 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 2026-05-20.

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.