Medical Device Manufacturer · US , Greenville , SC

Vidistar, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009

Total

Cleared

Denied

Vidistar, LLC has 2 FDA 510(k) cleared medical devices. Based in Greenville, US.

Historical record: 2 cleared submissions from 2009 to 2015. Primary specialty: Radiology.

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

510(k) submissions have been managed by Translational Science Solutions, LLC as regulatory consultant.

Vidistar, LLC is one of 18984 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Vidistar, LLC

2 devices

1-2 of 2

Data Source

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

Last updated: Sep 23, 2026