FDA applicant

Brentwood Medical Products, Inc.

Torrance, CA1 decision1997–19973 recalls

FDA records 1 decision for Brentwood Medical Products, Inc. (Torrance, CA) in 1997: 1 510(k) clearance. All are in product code DSI (Detector And Alarm, Arrhythmia). 3 recalls are 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 Brentwood Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Brentwood Medical Products, Inc. since 2007.

Recalls per year

3in 2010

2007high 3 (2010) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Brentwood Medical Products, 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 “Brentwood”

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

Brentwood Instruments, Inc. 21 Brentwood Medical Technology Corp. 7

Brentwood Medical Products, 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?

What has been recalled?

Other applicant names beginning “Brentwood”