# K210763: Inman Digital Clear Aligners

- Pathway: 510(k) (Traditional)
- Applicant: Inman Orthodontic Laboratories, Inc.
- Decided: Sep 29, 2021 after 198 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: 5 generations back to K780619 (1978). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K113618: Clearcorrect System, Clearcorrect, Inc. (2012) Summary page 4.

## Indications for use
Inman Digital Clear Aligners are indicated for the treatment of tooth malocclusions in patients with permanent dentition (i.e. all second molars). The Inman Digital Clear Aligners position teeth by way of continuous gentle force.

Source page: https://510kreport.com/device/K210763
Methodology: https://510kreport.com/methodology