# Cadent, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: DYW (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Ormco Corp.: 2 (https://510kreport.com/company/ormco)
- Great Lakes Orthodontics, Ltd.: 1 (https://510kreport.com/company/great-lakes-orthodontics)
- 3Shape A/S: 1 (https://510kreport.com/company/3shape-a-s)

## Its most-cited devices
- K082207: Orthocad IQ (2009), cited by 4

## Recent decisions
- K082207: Orthocad IQ (Oct 23, 2009)

Source page: https://510kreport.com/company/cadent