FDA applicant
Marken International, Inc.
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
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.
Planning a device like Marken International, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report