FDA applicant

Dio-Med Corp.

Cambridge Cb4 4ws England, GB7 decisions1981–19940 recalls

FDA records 7 decisions for Dio-Med Corp. (Cambridge Cb4 4ws England, GB) from 1981 to 1994: 7 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and DRS (Transducer, Blood-Pressure, Extravascular). 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 and plastic surgery panel, where it files most

How often FDA has decided Dio-Med Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dio-Med Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dio-Med Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?