FDA applicant

The Cyclotron Corp.

Mchenry, IL2 decisions1981–19810 recalls

FDA records 2 decisions for The Cyclotron Corp. (Mchenry, IL) in 1981: 2 510(k) clearances. All are in product code IWL (System, Radiation Therapy, Neutron, Medical). 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 The Cyclotron Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Cyclotron Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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The Cyclotron Corp.

Which product codes does it file in?

What has FDA decided for it lately?