Medical Device Manufacturer · US , Sandy Spring , MD

Angioslide, Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2010

Total

Cleared

Denied

Angioslide, Ltd. has 6 FDA 510(k) cleared medical devices. Based in Sandy Spring, US.

Historical record: 6 cleared submissions from 2010 to 2017. Primary specialty: Cardiovascular.

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

510(k) submissions have been managed by Ilya Burovoy- Regulatory and Quality Consulting as regulatory consultant.

Angioslide, Ltd. is one of 18924 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Angioslide, Ltd.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 14, 2026