FDA applicant

Kyron Clinical Imaging, Inc.

Wauwatosa, WI3 decisions2005–20060 recalls

FDA records 3 decisions for Kyron Clinical Imaging, Inc. (Wauwatosa, WI) from 2005 to 2006: 3 510(k) clearances. Most are in product codes LLZ (System, Image Processing, Radiological) and LNH (System, Nuclear Magnetic Resonance Imaging). Its devices cite 8 predicates, 1 of them its own earlier devices. 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 Kyron Clinical Imaging, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kyron Clinical Imaging, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Kyron Clinical Imaging, 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?