Asset Medikal is one of 37 FDA 510(k) medical device manufacturers from Turkey in the dataset, ranked by real submission volume.
Asset Medikal - FDA 510(k) Cleared Devices
Recent clearances: FlowArt® Vial Access Device Vented
1
Total
1
Cleared
0
Denied
Asset Medikal has 1 FDA 510(k) cleared medical devices. Based in Istanbul, TR.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Asset Medikal Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Arazy Group Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Asset Medikal
1 devices