FDA applicant

Mrx Corp.

Arlington, TX2 decisions1993–19940 recalls

FDA records 2 decisions for Mrx Corp. (Arlington, TX) from 1993 to 1994: 2 510(k) clearances. Most are in product codes ITY (Assembly, Tube Housing, X-Ray, Diagnostic) and JAK (System, X-Ray, Tomography, Computed). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Mrx Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mrx Corp.

Which product codes does it file in?

What has FDA decided for it lately?