Deep Blue Medical Advances, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Deep Blue Medical Advances, Inc. - FDA 510(k) Cleared Devices
Recent clearances: T-Line® Hernia Mesh, T-Line Hernia Mesh, T-Line Hernia Mesh
4
Total
4
Cleared
0
Denied
Deep Blue Medical Advances, Inc. has 4 FDA 510(k) cleared medical devices. Based in Durham, US.
Last cleared in 2023. Active since 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Deep Blue Medical Advances, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lince Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Deep Blue Medical Advances, Inc.
4 devices