FDA applicant

Hubinger Co.

Keokuk1 decision1978–19780 recalls

FDA records 1 decision for Hubinger Co. (Keokuk) in 1978: 1 original PMA approval. All are in product code KGP (Unnamed device). 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 Hubinger Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hubinger Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Hubinger Co.

Which product codes does it file in?

What has FDA decided for it lately?