Neux Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neux Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NXPRO Neuromuscular Electrical Stimulation Device
1
Total
1
Cleared
0
Denied
Neux Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Tampa, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Neux Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Devine Guidance International, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Neux Technologies, Inc.
1 devices