# Baxter Bentley Laboratories, Inc.

- Location (FDA's records): Irvine, CA
- FDA decisions: 3 (1988–1991): 3 510(k) clearances
- Product codes: DWD (1), DWF (1), DTZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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 that cite its devices most
- Edwards Lifesciences, LLC: 2 (https://510kreport.com/company/edwards-lifesciences)

## Its most-cited devices
- K905312: Duraflo II Heparin Treated Femoral Cannulae Models (1991), cited by 2

## Recent decisions
- K905311: Duraflo II Heparin Treated Suction Wands Var. Mod. (Jan 15, 1991)
- K905312: Duraflo II Heparin Treated Femoral Cannulae Models (Jan 15, 1991)
- K882892: Membrane Oxygenator (Sep 27, 1988)

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