The Linden Group Corp is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Linden Group Corp - FDA 510(k) Cleared Devices
Recent clearances: OptikView GUP2103CMI
2
Total
2
Cleared
0
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.
510(k) submissions have been managed by Qubyx Software Technologies, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - The Linden Group Corp
2 devices