# VitreQ BV

- Location (FDA's records): Vierpolders, NL
- FDA decisions: 2 (2019–2020): 2 510(k) clearances
- Product codes: HQB (1), HPS (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Katalyst Surgical, LLC: 1 (https://510kreport.com/company/katalyst-surgical)
- Peregrine Surgical, Ltd.: 1 (https://510kreport.com/company/peregrine-surgical)
- Dutch Ophthalmic USA, Inc.: 1 (https://510kreport.com/company/dutch-ophthalmic-usa)
- Keeler Limited: 1 (https://510kreport.com/company/keeler)

## Recent decisions
- K202038: CryoTreQ (Dec 30, 2020)
- K182646: Vitreq disposable laser probes, light fibers and Chandelier (May 1, 2019)

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