510(k) Report

FDA applicant

Global Medical Products, Ltd.

Woodbury, CT6 decisions1995–19970 recalls

FDA records 6 decisions for Global Medical Products, Ltd. (Woodbury, CT) from 1995 to 1997: 6 510(k) clearances. Most are in product codes DRC (Trocar) and BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)). No recall is linked to its devices.

FDA’s records also spell it “Global Medical Products, Inc.”.

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

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

How often FDA has decided Global Medical Products, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Global Medical Products, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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