FDA applicant

Biomedical Sensors, Inc.

Buckinghamshire, England, GB3 decisions1986–19970 recalls

FDA records 3 decisions for Biomedical Sensors, Inc. (Buckinghamshire, England, GB) from 1986 to 1997: 3 510(k) clearances. Most are in product codes CCC (Analyzer, Gas, Carbon-Dioxide, Partial…) and DRY (Monitor, Blood-Gas, On-Line, Cardiopulmonary…). No recall is linked to its devices.

FDA’s records also spell it “Biomedical Sensors, Ltd.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

How often FDA has decided Biomedical Sensors, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Biomedical Sensors, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Biomedical Sensors, Inc.

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?