Kaneka Americas Holding, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kaneka Americas Holding, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SurfRider 13 Microcatheter
1
Total
1
Cleared
0
Denied
Kaneka Americas Holding, Inc. has 1 FDA 510(k) cleared medical devices. Based in Newark, US.
Latest FDA clearance: Jan 2026. Active since 2026. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Kaneka Americas Holding, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mededge as regulatory consultant.
FDA 510(k) Regulatory Record - Kaneka Americas Holding, Inc.
1 devices