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Motive Knee System

FDA UDI

Class II (US FDA UDI)

by Motive Health, Inc.

Identity

Trade Name
Motive Knee System FDA UDI
Generic Name
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
Device Name
Motive Knee System, Right, Standard FDA UDI
Model / Reference
OT01-2001 FDA UDI
Description
Motive Knee System, Right, Standard FDA UDI

Identifiers

Catalog Number
OT01-2001 FDA UDI
Primary DI / UDI-DI
00850022650451 FDA UDI
FDA Product Code
IPF FDA UDI
GXY 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
882.1320 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 39.90 Inch FDA UDI

Category: Physical therapy transcutaneous neuromuscular electrical stimulation system

Motive Knee System by Motive Health, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physical therapy transcutaneous neuromuscular electrical stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Motive Health, Inc.

Sources (1)

  • FDA UDI 10afe461-35a0-4a50-8dc7-90d361518a7e 37 fields · synced May 30, 2026