Cleared Traditional

K222308 - Al Smile Aligner (FDA 510(k) Clearance)

Dec 2022
Decision
141d
Days
Class 2
Risk

K222308 is an FDA 510(k) clearance for the Al Smile Aligner. This device is classified as a Aligner, Sequential (Class II - Special Controls, product code NXC).

Submitted by Nanjing Jiahe Dental Technology Co., Ltd. (Nanjing, CN). The FDA issued a Cleared decision on December 20, 2022, 141 days after receiving the submission on August 1, 2022.

This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.5470. The Device Moves The Teeth By Continuous Gentle Force For Treatment Of Minor Tooth Malocclusion..

Submission Details

510(k) Number K222308 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 01, 2022
Decision Date December 20, 2022
Days to Decision 141 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF

Device Classification

Product Code NXC - Aligner, Sequential
Device Class Class II - Special Controls
CFR Regulation 21 CFR 872.5470
Definition The Device Moves The Teeth By Continuous Gentle Force For Treatment Of Minor Tooth Malocclusion.