# Prosenex

- Location (FDA's records): Leola, PA
- FDA decisions: 1 (2014–2014): 1 510(k) clearance
- Product codes: LQW (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (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
- Sensortek, Inc.: 1 (https://510kreport.com/company/sensortek)
- Somedic AB: 1 (https://510kreport.com/company/somedic)

## Recent decisions
- K141208: Dynamic Neuroscreening Device (Jul 23, 2014)

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