meddevicedb.com FDA Device Reference

Clear Moves Aligner

K241137 Class II Traditional
Decision Date
2024-08-01
Sponsor / Applicant
Clear Moves Aligners

Technical Specification

510(k) Submission ID K241137
Product Code NXC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 2024-08-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Clear Moves Aligner received FDA 510(k) clearance under submission number K241137, sponsored by Clear Moves Aligners. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2024-08-01.

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.