FDA applicant

Vascular Technologies, Ltd.

Ginot Shomron 44853, IL1 decision2000–20000 recalls

FDA records 1 decision for Vascular Technologies, Ltd. (Ginot Shomron 44853, IL) in 2000: 1 510(k) clearance. All are in product code FMF (Syringe, Piston). 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, general hospital panel, where it files most

How often FDA has decided Vascular Technologies, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vascular Technologies, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Vascular Technologies, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?