meddevicedb.com FDA Device Reference

6MS Invisible Aligner

K210652 Class II Traditional
Decision Date
2021-06-02
Sponsor / Applicant
Sms Opco, LLC

Technical Specification

510(k) Submission ID K210652
Product Code NXC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 2021-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

6MS Invisible Aligner received FDA 510(k) clearance under submission number K210652, sponsored by Sms Opco, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2021-06-02.

Classification & Regulation

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