Medical Device Manufacturer · US , Cedar Knolls , NJ

The Linden Group Corp - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2016

Total

Cleared

Denied

The Linden Group Corp has 2 FDA 510(k) cleared medical devices. Based in Cedar Knolls, US.

Historical record: 2 cleared submissions from 2016 to 2020. Primary specialty: Radiology.

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

FDA 510(k) cleared devices by The Linden Group Corp

2 devices

1-2 of 2