Dilon Technologies, Inc. is one of 21491 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dilon Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DILON 6800 ACELLA (ACELLA), DILON 2000, MODEL 2000-6X8 AND DILON 2000, MODEL 2000-5X5
2
Total
2
Cleared
0
Denied
Dilon Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Stillwater, US.
Historical record: 2 cleared submissions from 1999 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Dilon Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dilon Technologies, Inc.
2 devices