FDA applicant

Dbt Medical, Ltd.

Witney,0x8 7az, GB5 decisions1985–19850 recalls

FDA records 5 decisions for Dbt Medical, Ltd. (Witney,0x8 7az, GB) in 1985: 5 510(k) clearances. Most are in product codes EXB (Collector, Ostomy) and EXJ (Device, Incontinence, Urosheath Type, Sterile). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Dbt Medical, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dbt Medical, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?