FDA applicant

Styker Instruments

Kalamazoo, MI1 decision2002–20020 recalls

FDA records 1 decision for Styker Instruments (Kalamazoo, MI) in 2002: 1 510(k) clearance. All are in product code IYE (Accelerator, Linear, Medical). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Styker Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Styker Instruments

Which product codes does it file in?

What has FDA decided for it lately?