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INNOVATIVE NEUROTRONICS INC.

Last updated September 17, 2026

Information

Device	Model / Reference	Registries	Class	Status
WalkAnalyst Software Kit	20-0603	FDA UDI	Class II	Active
WalkAide Unit	20-0100	FDA UDI	Class II	Active
WalkAide 1.875 Premium Electrodes - pkg of 4	20-0540	FDA UDI	Class II	Active
WalkAide Kit for Japan	21-1000	FDA UDI	Class II	Active
WalkAide Kit for Demo Use	20-1002	FDA UDI	Class II	Active
WalkAide 1.25 Premium Electrodes - pkg of 4	20-0521	FDA UDI	Class II	Active
WalkAide Kit	20-1000	FDA UDI	Class II	Active
WalkAide Electrodes - package of 4	20-0500	FDA UDI	Class II	Active
WalkAide	20-0590	FDA UDI	Class II	Active
WalkAide	20-0580	FDA UDI	Class II	Active
WalkLink Unit	20-0310	FDA UDI	Class II	Active
WalkAide	20-0591	FDA UDI	Class II	Active
WalkLink System ((Clinician Kit)	20-0300	FDA UDI	Class II	Active
Walkaide System	K140886	FDA 510(k)	Class II	Active
Walkaide System	K123972	FDA 510(k)	Class II	Active
Walkaide System, Models 20-0100, 20-0310, 20-1000	K052329	FDA 510(k)	Class II	Active

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Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Aug 6, 2008	Z-1435-2009	—	terminated	Knob responsible for regulating the amount of stimulation administered by the WalkAide System control unit may fall off while device is in use.