meddevicedb.com FDA Device Reference

Nightwear Aligners

K221537 Class II Traditional
Decision Date
2023-04-05
Sponsor / Applicant
Smylio, Inc.

Technical Specification

510(k) Submission ID K221537
Product Code NXC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 2023-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Nightwear Aligners received FDA 510(k) clearance under submission number K221537, sponsored by Smylio, 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 2023-04-05.

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.