# K220140: ClearCorrect System

- Pathway: 510(k) (Traditional)
- Applicant: Clearcorrect, LLC
- Decided: Oct 5, 2022 after 260 days
- Product code: NXC (Aligner, Sequential)
- Device class: 2
- Regulation: 21 CFR 872.5470
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K780619 (1978). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K143630: Invisalign System, Align Technology, Inc. (2015) Summary page 4.

## Indications for use
The ClearCorrect System is indicated for the alignment of teeth during orthodontic treatment of tooth malocclusion.

Source page: https://510kreport.com/device/K220140
Methodology: https://510kreport.com/methodology