# Jostra Bentley

- Location (FDA's records): Austin, TX
- FDA decisions: 3 (1995–1999): 3 510(k) clearances
- Product codes: DWC (1), DTZ (1), DPW (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 4 (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
- Avecor Cardiovascular, Inc.: 1 (https://510kreport.com/company/avecor-cardiovascular)
- Janus Biomedical, Inc.: 1 (https://510kreport.com/company/janus-biomedical)

## Firms that cite its devices most
- Maquet Cardiopulmonary, AG: 2 (https://510kreport.com/company/maquet-cardiopulmonary)
- Jostra AG: 1 (https://510kreport.com/company/jostra)
- Polystan A/S: 1 (https://510kreport.com/company/polystan-a-s)

## Its most-cited devices
- K992559: Hollow Fiber Membrane Oygenator Quadrox Hmo 1010 (1999), cited by 4

## Recent decisions
- K992559: Hollow Fiber Membrane Oygenator Quadrox Hmo 1010 (Sep 20, 1999)
- K984338: Jostra HL-20 Twin Pump (Aug 19, 1999)
- K945720: Jostra HL-15 Modular Heart-Lung Machine (Hereinafter Called the HL-15 or the Device (Mar 29, 1995)

Source page: https://510kreport.com/company/jostra-bentley