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NexWave

FDA UDI

Class II (US FDA UDI)

by Zynex Medical, Inc.

Identity

Trade Name
NexWave FDA UDI
Generic Name
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
Device Name
An electrotherapy device which offers the user a choice of three operational modes: IFC, TENS, and NMES. FDA UDI
Model / Reference
400400 FDA UDI
Description
An electrotherapy device which offers the user a choice of three operational modes: IFC, TENS, and NMES. FDA UDI

Identifiers

Primary DI / UDI-DI
00852670007007 FDA UDI
510(k) Number
K111279 FDA UDI
FDA Product Code
IPF FDA UDI
GZJ FDA UDI
LIH FDA UDI
GMDN Term
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5850 FDA UDI
882.5890 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Physical therapy transcutaneous neuromuscular electrical stimulation systemAnalgesic transcutaneous electrical nerve stimulation systemInterferential electrical stimulation system

NexWave by Zynex Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Interferential electrical stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zynex Medical, Inc.

Sources (1)

  • FDA UDI 01e089b2-2356-4639-8db4-d6ac394f8c87 35 fields · synced May 30, 2026