Senseonics, Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Senseonics, Incorporated - FDA 510(k) Cleared Devices
Recent clearances: Eversense 365 Continuous Glucose Monitoring (CGM) System
2
Total
1
Cleared
1
Denied
Senseonics, Incorporated has 1 FDA 510(k) cleared medical devices. Based in Geramantown, US.
Latest FDA clearance: Sep 2024. Active since 2024. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Senseonics, Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Senseonics, Incorporated
2 devices