FDA applicant

Vascular Flow Technologies, Ltd.

Dundee, GB4 decisions2014–20250 recalls

FDA records 4 decisions for Vascular Flow Technologies, Ltd. (Dundee, GB) from 2014 to 2025: 4 510(k) clearances. All are in product code DSY (Prosthesis, Vascular Graft, Of 6mm And Greater…). Its devices cite 5 predicates, 2 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Vascular Flow Technologies Limited”.

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

FDA decisions per year

1in 2025

2014high 2 (2014) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Vascular Flow Technologies, Ltd. by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Vascular Flow Technologies, 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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Vascular Flow Technologies, Ltd.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?