meddevicedb.com FDA Device Reference

Avex CX2

K152779 Class II Special
Decision Date
2015-11-25
Sponsor / Applicant
Opal Orthodontics by Ultradent Products

Technical Specification

510(k) Submission ID K152779
Product Code NJM
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 2015-11-25
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Avex CX2 received FDA 510(k) clearance under submission number K152779, sponsored by Opal Orthodontics by Ultradent Products. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-11-25.

Classification & Regulation

This clearance is catalogued under FDA product code NJM and 21 CFR 872.5470, within the Dental review panel as a Class II device.