FDA applicant

Medx, Inc.

Arlington Heights, IL11 decisions1987–20081 recall

FDA records 11 decisions for Medx, Inc. (Arlington Heights, IL) from 1987 to 2008: 11 510(k) clearances. Most are in product codes IYX (Camera, Scintillation (Gamma)) and KPS (System, Tomography, Computed, Emission). Its devices cite 5 predicates, 0 of them its own earlier devices. 1 recall is linked to its devices.

FDA’s records also spell it “Medx Corp.”.

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 Medx, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2007high 1 (2007) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

1in 2013

2007high 1 (2013) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Medx, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Medx”

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

Medx Electronics, Inc. 6 Medx-Set, Ltd. 1

Medx, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Medx”