Cleared Traditional

K240038 - Clear Moves Aligners (FDA 510(k) Clearance)

Apr 2024
Decision
90d
Days
Class 2
Risk

K240038 is an FDA 510(k) clearance for the Clear Moves Aligners. This device is classified as a Aligner, Sequential (Class II - Special Controls, product code NXC).

Submitted by Space Maintainers Laboratories (Sml) (Chatsworth, US). The FDA issued a Cleared decision on April 4, 2024, 90 days after receiving the submission on January 5, 2024.

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 K240038 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 05, 2024
Decision Date April 04, 2024
Days to Decision 90 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.