meddevicedb.com FDA Device Reference

Toothsi, Smilealigners

K223338 Class II Traditional
Decision Date
2023-02-09
Sponsor / Applicant
Makeo Healthcare Technologies Private Limited

Technical Specification

510(k) Submission ID K223338
Product Code NXC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 2023-02-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Toothsi, Smilealigners received FDA 510(k) clearance under submission number K223338, sponsored by Makeo Healthcare Technologies Private Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2023-02-09.

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.