Sonostik, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sonostik, LLC - FDA 510(k) Cleared Devices
Recent clearances: SonoStik Guide Wire Introducer
2
Total
2
Cleared
0
Denied
Sonostik, LLC has 2 FDA 510(k) cleared medical devices. Based in N Potomac, US.
Latest FDA clearance: Nov 2024. Active since 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Sonostik, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Keystone Regulatory Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Sonostik, LLC
2 devices