FDA applicant

Brentwood Medical Technology Corp.

Torrance, CA7 decisions2000–20111 recall

FDA records 7 decisions for Brentwood Medical Technology Corp. (Torrance, CA) from 2000 to 2011: 7 510(k) clearances. Most are in product codes DPS (Electrocardiograph) and DXN (System, Measurement, Blood-Pressure…). Its devices cite 7 predicates, 0 of them its own earlier devices. 1 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 Brentwood Medical Technology Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2007high 1 (2010) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

1in 2026

2007high 1 (2026) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Brentwood Medical Technology Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Brentwood Medical Technology Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

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 Products, Inc. 1

Brentwood Medical Technology Corp.

Which product codes does it file in?

Whose devices does it build on?

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”