FDA applicant

Med-Tec,Inc.

Orange City, IA8 decisions1998–20040 recalls

FDA records 8 decisions for Med-Tec,Inc. (Orange City, IA) from 1998 to 2004: 8 510(k) clearances. Most are in product codes IYE (Accelerator, Linear, Medical) and JAI (Couch, Radiation Therapy, Powered). 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-Tec,Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Med-Tec,Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Med-Tec,Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?