FDA applicant

Kermath Mfg. Corp.

Mchenry, IL5 decisions1977–19870 recalls

FDA records 5 decisions for Kermath Mfg. Corp. (Mchenry, IL) from 1977 to 1987: 5 510(k) clearances. Most are in product codes KPR (System, X-Ray, Stationary) and KPQ (System, Simulation, Radiation Therapy). 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 Kermath Mfg. Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kermath Mfg. Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Kermath Mfg. Corp.

Which product codes does it file in?

What has FDA decided for it lately?