NXPro

by Neux Technologies, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 8 Jun 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 8 Jun 2026. What this means

Regulatory status

as of registry sync 8 Jun 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00199284950719 UDI-DI	Date19 Aug 2025Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 8 Jun 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name: Physical therapy transcutaneous neuromuscular electrical stimulation system
Model / Reference: NXPro

Primary DI / UDI-DI: 00199284950719
510(k) Number: K191181
FDA Product Code: NGX
GMDN Term: Physical therapy transcutaneous neuromuscular electrical stimulation system

Device Class: Class II
Regulation Number: 890.5850
GUDID distribution status: In Commercial Distribution

Other devices from Neux Technologies, Inc.

NXPRO Neuromuscular Electrical Stimulation Device

Class II

Properties

Over-the-Counter
Serial Number
Manufacturing Date

Other properties (11)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Lot / Batch Number: No
Expiration Date: No