Medical Device Manufacturer · US , Chicago , IL

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

2 submissions · 2 cleared · Since 2006

Recent clearances: DIGDOP ULTRASOUND SYSTEM, BABYBEAT CORDLESS

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

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

2 devices

1-2 of 2

Cleared Apr 08, 2009

DIGDOP ULTRASOUND SYSTEM

Radiology · 44d

Cleared May 04, 2006

BABYBEAT CORDLESS

Radiology · 15d

Data Source

Sourced from the FDA 510(k) public files . 176,583 total devices indexed.

Last updated: Sep 27, 2026