Dexcowin Global, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dexcowin Global, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Cocoon Solo (DX-7020s)
1
Total
1
Cleared
0
Denied
Dexcowin Global, Inc. has 1 FDA 510(k) cleared medical devices. Based in Pasadena, US.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Dexcowin Global, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mtech Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Dexcowin Global, Inc.
1 devices