Sureax Medical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sureax Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: SureAx-Guide™
1
Total
1
Cleared
0
Denied
Sureax Medical, LLC has 1 FDA 510(k) cleared medical devices. Based in San Diego, US.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Sureax Medical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Starlight Medical Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Sureax Medical, LLC
1 devices