510(k) Report

FDA applicant

Marken International, Inc.

Bozeman, MT1 decision2002–20020 recalls

FDA records 1 decision for Marken International, Inc. (Bozeman, MT) in 2002: 1 510(k) clearance. All are in product code IOR (Wheelchair, Mechanical). 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, physical medicine panel, where it files most

How often FDA has decided Marken International, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Marken International, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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