meddevicedb.com FDA Device Reference

SmileSeries

K221097 Class II Traditional
Decision Date
2022-07-14
Sponsor / Applicant
Ordont Orthodontic Laboratories, Inc.

Technical Specification

510(k) Submission ID K221097
Product Code NXC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 2022-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SmileSeries received FDA 510(k) clearance under submission number K221097, sponsored by Ordont Orthodontic Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2022-07-14.

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.