Genesis Software Innovations is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Genesis Software Innovations - FDA 510(k) Cleared Devices
Recent clearances: Preview Shoulder, Preview Shoulder
2
Total
2
Cleared
0
Denied
Genesis Software Innovations has 2 FDA 510(k) cleared medical devices. Based in Grand Rapids, US.
Latest FDA clearance: Apr 2024. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Genesis Software Innovations Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Genesis Software Innovations
2 devices