FDA applicant

Medicor USA, Ltd.

Columbus, OH14 decisions1978–19860 recalls

FDA records 14 decisions for Medicor USA, Ltd. (Columbus, OH) from 1978 to 1986: 14 510(k) clearances. Most are in product codes IYB (Tube Mount, X-Ray, Diagnostic) and IXR (Table, Radiographic, Tilting). 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 Medicor USA, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medicor USA, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medicor USA, 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 “Medicor”

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

Medicor Corp. 1

Medicor USA, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Medicor”