FDA applicant

W.G. Whitney Corp.

Mchenry, IL7 decisions1977–19840 recalls

FDA records 7 decisions for W.G. Whitney Corp. (Mchenry, IL) from 1977 to 1984: 7 510(k) clearances. Most are in product codes EFQ (Gauze/Sponge, Internal) and KDD (Kit, Surgical Instrument, Disposable). 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for W.G. Whitney Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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W.G. Whitney Corp.

Which product codes does it file in?

What has FDA decided for it lately?