Medical Device Manufacturer · US , Anaheim , CA

Vascular Medcure, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2019

Total

Cleared

Denied

Vascular Medcure, Inc. has 5 FDA 510(k) cleared medical devices. Based in Anaheim, US.

Historical record: 5 cleared submissions from 2019 to 2020. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Vascular Medcure, Inc. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Hogan Lovells US LLP and Hogan & Lovells U.S. Lpp.

Vascular Medcure, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Vascular Medcure, Inc.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: May 28, 2026