# Cadwell

- Location (FDA's records): Kennewick, WA
- FDA decisions: 2 (2013–2014): 2 510(k) clearances
- Product codes: OMB (1), PDQ (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 1 (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 whose devices it cites most
- Persyst Development Corporation: 1 (https://510kreport.com/company/persyst-development)

## Firms that cite its devices most
- Biomet Spine (Aka Ebi, LLC): 1 (https://510kreport.com/company/biomet-spine-aka-ebi)

## Its most-cited devices
- K123589: Cadwell Disposable Probe Handle (2013), cited by 1

## Recent decisions
- K140552: Cadwell Spike and Seizure Detector (Jul 23, 2014)
- K123589: Cadwell Disposable Probe Handle (Mar 19, 2013)

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