FDA applicant

Lic-Orthion

Mchenry, IL17 decisions1983–19890 recalls

FDA records 17 decisions for Lic-Orthion (Mchenry, IL) from 1983 to 1989: 17 510(k) clearances. Most are in product codes ILC (Utensil, Eating) and KNX (Collector, Urine, (And Accessories) For…). 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, physical medicine panel, where it files most

How often FDA has decided Lic-Orthion’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lic-Orthion since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Lic-Orthion

Which product codes does it file in?

What has FDA decided for it lately?