Medical Device Manufacturer · US , Chicago , IL

The Newman Group, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2006

Total

Cleared

Denied

The Newman Group, LLC has 2 FDA 510(k) cleared medical devices. Based in Chicago, US.

Historical record: 2 cleared submissions from 2006 to 2009. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - The Newman Group, LLC

2 devices

1-2 of 2

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 28, 2026