FDA Device Intelligence
Home › INNOVATIVE NEUROTRONICS, INC. › WalkAide Kit for Demo Use

WalkAide Kit for Demo Use

INNOVATIVE NEUROTRONICS, INC. · Model 20-1002 · UDI-DI 00858184006048

GZI Prescription
1
510(k) clearances
50
Adverse events (1 deaths)
2
Recalls
40
Facilities

Description

The WalkAide is a battery-operated, single channel electrical stimulator that is used to improve walking ability. It stimulates a foot lift at the correct time during walking. A foot drop occurs when a person connot lift the foot on their own. This results in the foot slapping on the floor or the toes dragging during walking. The WalkAide stimulates a nerve as it passes below the knee and activates the muscles that raise the foot.The WalkAide Patient Kit includes a WalkAide Control Unit, a WalkAide cuff, and an electrode lead cable. A foot sensor is an optional item

Recalls

DateFirmReason
2022-07-19Myolyn Inc.Screws mounting an internal power supply may come loose during shipping resulting in increased risk of high voltage electrical shock.
2008-08-06Innovative Neurotronics, Inc.Knob responsible for regulating the amount of stimulation administered by the WalkAide System control unit may fall off while device is in use.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.