Neks Technologies, Inc. is one of 23415 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neks Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: D-CARIE/DETECTAR, MODELS N121, N123, N133, N134, N135 & N138, D-CARIE, MODEL N121-M1
2
Total
2
Cleared
0
Denied
Neks Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Durham, US.
Historical record: 2 cleared submissions from 2005 to 2007. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Neks Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neks Technologies, Inc.
2 devices