FDA applicant

Baxter Bentley Laboratories, Inc.

Irvine, CA3 decisions1988–19910 recalls

FDA records 3 decisions for Baxter Bentley Laboratories, Inc. (Irvine, CA) from 1988 to 1991: 3 510(k) clearances. Most are in product codes DWD (Suction Control, Intracardiac, Cardiopulmonary…) and DWF (Catheter, Cannula And Tubing, Vascular…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Baxter Bentley Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Baxter Bentley Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Baxter Bentley Laboratories, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Baxter”

FDA records each applicant name separately; these may or may not be the same firm.

Baxter Healthcare Corp 574 Baxter Diagnostics, Inc. 72 Baxter Edwards 11 Baxter Healthcare Corportation 3 Baxter Healthcare Corporation - Renal Division 2 Baxter/ Synovis Micro Companies Alliance, Inc. 2 Baxter Healthcare Corp/ Excel Medical 1 Baxter Centre For Medical Research 1 Baxter Healthcare Corproration 1 Baxter Corp. 1 Baxter Interwoven Offsite 1 Baxter Healthcare Corp., Bioscience 1

Baxter Bentley Laboratories, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Baxter”