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.

Regulatory submissions have been managed by Qubyx , Ltd. and Qubyx Software Technologies, Inc..

The Linden Group Corp is one of 13424 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - The Linden Group Corp

2 devices

1-2 of 2

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: May 29, 2026