Medical Device Manufacturer · US , Cedar Knolls , NJ

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

2 submissions · 2 cleared · Since 2016

Recent clearances: OptikView GUP2103CMI, DIVA ZSP2105CMI with QUBYX PerfectLum bundle

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

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

2 devices

1-2 of 2

Cleared Mar 16, 2020

OptikView GUP2103CMI

Radiology · 264d

Cleared Feb 25, 2016

DIVA ZSP2105CMI with QUBYX PerfectLum bundle

Radiology · 20d

Data Source

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

Last updated: May 29, 2026