NEUX TECHNOLOGIES, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30171467423017146742NEUX TECHNOLOGIES, INC.1N2026-01-01802 E Whiting Street Tampa FL US 33602

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00199284950719NXPro - The NXPro is an FDA-cleared, Class II, over-the-counter medical device that can be sold directly to healthy consumers without a prescription. This means any healthy individual (free from designated contraindications) can purchase and use this device on themselves or other health individuals for muscle conditioning, ensuring adequate safety and effectiveness in delivering advanced neuromuscular stimulation.561-510-1882pauletteb@neuxtec.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2740801259531255K191181NXPRO Neuromuscular Electrical Stimulation DeviceNGX2019-10-11

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
NGX12019-10-11

PMN#

GUDID#