FDA applicant

Trimline Medical Products Corp.

Branchburg, NJ2 decisions2008–20090 recalls

FDA records 2 decisions for Trimline Medical Products Corp. (Branchburg, NJ) from 2008 to 2009: 2 510(k) clearances. All are in product code DXQ (Blood Pressure Cuff). 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 Trimline Medical Products Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2008high 1 (2008) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Trimline Medical Products Corp. by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Trimline Medical Products Corp.

Which product codes does it file in?

What has FDA decided for it lately?