FDA applicant

Med Corp.

Ames, IA1 decision1995–19950 recalls

FDA records 1 decision for Med Corp. (Ames, IA) in 1995: 1 510(k) clearance. All are in product code EAK (Screen, Leaded, Operator Radiation Protector). 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 Med Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Med Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Med Corp.’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

Med Corp.

Which product codes does it file in?

What has FDA decided for it lately?