# K182329: SureCure Orthodontic Aligner System

- Pathway: 510(k) (Traditional)
- Applicant: Digital Orthodontic Care
- Decided: Nov 8, 2018 after 72 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.
3 later devices descend from it; 1 cites it directly.
0 of 11 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.

## Most influential descendants
- K212803: DailyMate Orthodontic Aligner System (2022), 2 descendants of its own
- K233356: Illusion Aligner Pro: Illusion Aligner FLX (2024), 1 descendant of its own
- K251454: Clear Aligner (SCF-3348) (2026), 0 descendants of its own

## Indications for use
The SureCure Orthodontic Aligner System is indicated for the treatment of tooth malocclusion in patients with permanent dentition. The aligner system repositions teeth by way of continuous gentle force.

Source page: https://510kreport.com/device/K182329
Methodology: https://510kreport.com/methodology