# Liquet Medical, Inc.

- Location (FDA's records): Glen Allen, VA
- FDA decisions: 2 (2024–2026): 2 510(k) clearances
- Product codes: QEY (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (1 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
- Thrombolex, Inc.: 1 (https://510kreport.com/company/thrombolex)
- Edwards Lifesciences, LLC: 1 (https://510kreport.com/company/edwards-lifesciences)

## Its most-cited devices
- K241851: Versus™ Catheter  (VS110-8B) (2024), cited by 1

## Recent decisions
- K260149: Versus™ Catheter  (VS110-9NB) (Feb 17, 2026)
- K241851: Versus™ Catheter  (VS110-8B) (Nov 25, 2024)

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