FDA applicant

The Kinder Co.

Ypsilanti, MI1 decision1987–19870 recalls

FDA records 1 decision for The Kinder Co. (Ypsilanti, MI) in 1987: 1 510(k) clearance. All are in product code GAX (Tourniquet, Nonpneumatic). 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 The Kinder Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Kinder Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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The Kinder Co.

Which product codes does it file in?

What has FDA decided for it lately?