Smartsurgn Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Smartsurgn Incorporated - FDA 510(k) Cleared Devices
Recent clearances: SmartSurgN Visualization System
1
Total
1
Cleared
0
Denied
Smartsurgn Incorporated has 1 FDA 510(k) cleared medical devices. Based in San Jose, US.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Smartsurgn Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Smartsurgn Incorporated
1 devices