FDA applicant

Casmed UK

Surrey, GB1 decision2000–20000 recalls

FDA records 1 decision for Casmed UK (Surrey, GB) in 2000: 1 510(k) clearance. All are in product code MQE (Needle, Assisted Reproduction). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Casmed UK’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Casmed UK since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Casmed UK

Which product codes does it file in?

What has FDA decided for it lately?