Dilon Technologies, LLC is one of 21453 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dilon Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: GAMMALOC SYSTEM, MODEL 03-00001
1
Total
1
Cleared
0
Denied
Dilon Technologies, LLC has 1 FDA 510(k) cleared medical devices. Based in Newport News, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Dilon Technologies, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dilon Technologies, LLC
1 devices