FDA applicant

Murex Corp.

Norcross, GA5 decisions1986–19860 recalls

FDA records 5 decisions for Murex Corp. (Norcross, GA) in 1986: 5 510(k) clearances. Most are in product codes GTZ (Antisera, All Groups, Streptococcus Spp.) and DQX (Wire, Guide, Catheter). 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 Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Murex Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Murex Corp. 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 Diagnostics, Inc. 2 Murex Biotech, Ltd. 1 Murex Diagnostics Limitd 1

Murex Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Murex”