FDA applicant

K. W. Griffen Co.

Stamford, CT4 decisions1987–19960 recalls

FDA records 4 decisions for K. W. Griffen Co. (Stamford, CT) from 1987 to 1996: 4 510(k) clearances. Most are in product codes NAD (Dressing, Wound, Occlusive) and GEC (Brush, Scrub, Operating-Room). 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 K. W. Griffen Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for K. W. Griffen Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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K. W. Griffen Co.

Which product codes does it file in?

What has FDA decided for it lately?