FDA applicant

Clinipad Corp.

Mchenry, IL16 decisions1980–19940 recalls

FDA records 16 decisions for Clinipad Corp. (Mchenry, IL) from 1980 to 1994: 16 510(k) clearances. Most are in product codes FRG (Wrap, Sterilization) and KMF (Bandage, Liquid). 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, general hospital panel, where it files most

How often FDA has decided Clinipad Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Clinipad Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Clinipad Corp.

Which product codes does it file in?

What has FDA decided for it lately?