meddevicedb.com FDA Device Reference

Orthodontic Facemask

K202855 Class II Traditional
Decision Date
2021-06-21
Sponsor / Applicant
Ita.O Italian Orthodontic System S.R.L.

Technical Specification

510(k) Submission ID K202855
Product Code DZB
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5500
Decision Date 2021-06-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Orthodontic Facemask received FDA 510(k) clearance under submission number K202855, sponsored by Ita.O Italian Orthodontic System S.R.L.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2021-06-21.

Classification & Regulation

This clearance is catalogued under FDA product code DZB and 21 CFR 872.5500, within the Dental review panel as a Class II device.