FDA UDI In Commercial Distribution 🇺🇸 United States

NXPro

DI: 00199284950719 · Model: NXPro · Neux Technologies, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NXPro
Primary DI
00199284950719
Version / Model
NXPro
Company Name
Neux Technologies, Inc.
Labeler DUNS
080409222
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-08-19
Public Version
2
Public Version Date
2025-09-09
Public Version Status
Update
Public Device Record Key
caf8bfd1-2dad-4510-891a-aa4a7154a34b

Device Description

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.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NGX Stimulator, Muscle, Powered, For Muscle Conditioning

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 00199284950719

Customer Contacts

Phone
561-510-1882

Premarket Submissions

Submission Number Supplement Number
K191181 000