# Piolax Medical Devices, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 1 (1998–1998): 1 510(k) clearance
- Product codes: DQX (1)
- Predicates its devices cite: 1 (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
- Terumo Medical Corp.: 1 (https://510kreport.com/company/terumo-medical)

## Recent decisions
- K980977: Piolax Hydrophilic Guidewire (Oct 27, 1998)

Source page: https://510kreport.com/company/piolax-medical-devices