MyndMove

MyndTec Inc · Model MyndMove Mobile Cart · UDI-DI 00692520202769

GZI Prescription

510(k) clearances

Adverse events (1 deaths)

Recalls

Facilities

Recalls

Date	Firm	Reason
2022-07-19	Myolyn Inc.	Screws mounting an internal power supply may come loose during shipping resulting in increased risk of high voltage electrical shock.
2008-08-06	Innovative 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.

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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.