Foot Drop System XFT-2001D – Lower Limb Training Exercise

The XFT-2001D is a Class II orthotic trainer designed to help people with foot drop caused by neurological conditions or nerve injury. It is intended for use in rehabilitation settings and at home under clinical guidance to improve lower limb movement and mobility.

The device uses functional electrical stimulation (FES) guided by advanced MEMS sensors and intelligent algorithms to detect leg swing angle and pace, then precisely time and control stimulation to assist dorsiflexion during gait.

It is commonly used for foot drop related to stroke (CVA), multiple sclerosis (MS), spinal cord injury (SCI), traumatic brain injury (TBI), brain tumor, cerebral palsy (CP) and other brain or spinal disorders that affect ankle dorsiflexion.

Yes. The XFT-2001D is classified as a Class II medical device and carries CE marking and ISO 13485 certification, indicating it meets applicable regulatory and quality management standards.

The device is compact and lightweight with dimensions of 111 x 62 x 22 mm and a net weight of approximately 63 g, making it suitable for both clinical and home use.

The XFT-2001D is battery powered. Specific battery type and expected runtime are provided in the product user manual. Batteries are not covered under the standard 5-year warranty.

Basic setup typically includes attaching the device and electrodes/straps per the user manual, configuring stimulation settings, and performing an initial calibration while standing or walking. Setup and parameter tuning should be performed by or under the supervision of a trained clinician or therapist.

Yes. Clinical assessment, prescription, and fitting by a qualified rehabilitation professional are recommended to ensure appropriate parameters, safe use, and optimal therapeutic outcomes.

Common precautions include implanted electronic devices (e.g., pacemakers), pregnancy, active infection or open wounds at the electrode site, uncontrolled epilepsy, or severe sensory deficits. Always consult a clinician and refer to the device safety manual for complete contraindications and warnings.

Yes. The unit's compact, lightweight design makes it suitable for home use following clinician instruction, training, and ongoing follow-up to monitor progress and adjust settings as needed.

Keep the device dry and clean by wiping with a soft, damp cloth and mild disinfectant as described in the manual. Inspect leads, electrodes, straps and connectors regularly and replace consumables (electrodes, batteries) per manufacturer guidance.

The product includes a 5-year warranty covering manufacturing defects and device malfunction under normal use. Consumables such as batteries and electrodes are typically excluded. Check the warranty terms provided by the supplier for full details and registration requirements.

The device's compact design allows it to be used with many AFOs and types of footwear, but compatibility depends on the specific AFO and shoe. A clinician should evaluate fit and function to ensure the device does not interfere with orthosis performance.

The XFT-2001D applies established FES principles and sensor-controlled stimulation commonly used in lower-limb rehabilitation. For device-specific clinical data, performance studies, or published research, consult the manufacturer's documentation or contact their clinical support team.

Contact the manufacturer's authorized distributor or supplier to place an order, arrange demonstrations, request clinician training, or obtain spare parts and technical support. The supplier can provide information about local service, warranty registration and user training options.