Medical Device Manufacturer · US , Menlo Park , CA

Endovascular Engineering - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2023

Total

Cleared

Denied

Endovascular Engineering has 2 FDA 510(k) cleared medical devices. Based in Menlo Park, US.

Latest FDA clearance: Sep 2026. Active since 2023. Primary specialty: Cardiovascular.

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

Endovascular Engineering is one of 16546 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Endovascular Engineering

2 devices

1-2 of 2