Kaneka Pharma America, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kaneka Pharma America, LLC - FDA 510(k) Cleared Devices
Recent clearances: i-ED COIL
4
Total
4
Cleared
0
Denied
Kaneka Pharma America, LLC has 4 FDA 510(k) cleared medical devices. Based in Hudson, US.
Historical record: 4 cleared submissions from 2010 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Kaneka Pharma America, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by KANEKA Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - Kaneka Pharma America, LLC
4 devices