Medical Device Manufacturer · US , Menlo Park , CA

Jupiter Endovascular - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025

Total

Cleared

Denied

Jupiter Endovascular has 1 FDA 510(k) cleared medical devices. Based in Menlo Park, US.

Latest FDA clearance: Sep 2025. Active since 2025. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Jupiter Endovascular Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Jupiter Endovascular

1 devices

1-1 of 1