Dynex Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dynex Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DYNEX SmartPLEX MMRV IgG Assay Kit
1
Total
1
Cleared
0
Denied
Dynex Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Chantilly, US.
Last cleared in 2023. Active since 2023. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Dynex Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dynex Technologies, Inc.
1 devices