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WalkLink Unit

FDA UDI

Class II (US FDA UDI)

by Innovative Neurotronics Inc.

Identity

Trade Name
WalkLink Unit FDA UDI
Generic Name
Gait-enhancement electrical stimulation system, external FDA UDI
Device Name
Provides a wireless connection between the WalkAide and a computer, and also allows manual stimulation during walking trials via the Hand Switch. FDA UDI
Model / Reference
20-0310 FDA UDI
Description
Provides a wireless connection between the WalkAide and a computer, and also allows manual stimulation during walking trials via the Hand Switch. FDA UDI

Identifiers

Primary DI / UDI-DI
00858184006055 FDA UDI
510(k) Number
K140886 FDA UDI
FDA Product Code
GZI FDA UDI
GMDN Term
Gait-enhancement electrical stimulation system, external FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5810 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Gait-enhancement electrical stimulation system, external

WalkLink Unit by Innovative Neurotronics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gait-enhancement electrical stimulation system, external.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI edf57b08-9f27-4463-8c03-3eb6d518480e 36 fields · synced Jun 8, 2026