Neux Technologies, Inc.
United Statesfrom the FDA registration address FDA FEI 3017146742
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3017146742
- DUNS number
- 080409222
- Address
- 802 E Whiting Street, Tampa, FL, 33602
- [email protected]
- Phone
- 561-510-1882
Frequently asked questions
How many devices does Neux Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Neux Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neux Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Neux Technologies, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Neux Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Neux Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neux Technologies, Inc. in the registry?
The most recently registered devices listed for Neux Technologies, Inc. include NXPro and NXPRO Neuromuscular Electrical Stimulation Device.