Smartsurgn, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Smartsurgn, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SmartSurgN Visualization System, AirSurgN Insufflator (10030/AirSurgN)
2
Total
2
Cleared
0
Denied
Smartsurgn, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Jose, US.
Latest FDA clearance: Apr 2026. Active since 2025. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Smartsurgn, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Smartsurgn, Inc.
2 devices