FDA applicant

Murex Biotech, Ltd.

Dartford,Kent, GB1 decision1997–19970 recalls

FDA records 1 decision for Murex Biotech, Ltd. (Dartford,Kent, GB) in 1997: 1 510(k) clearance. All are in product code GMZ (Antigens, All Types, Escherichia Coli). 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, microbiology panel, where it files most

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

FDA decisions per year

No FDA decision for Murex Biotech, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Murex”

FDA records each applicant name separately; these may or may not be the same firm.

Murex Corp. 5 Murex Diagnostics, Inc. 2 Murex Diagnostics Limitd 1

Murex Biotech, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Murex”