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Tyromotion GmbH: Robotic Hand and Gait Rehabilitation Systems
Assess Tyromotion's Amadeo and Lexo rehabilitation systems, a model-specific EU MDR announcement, clinical software responsibilities, regional support, and procurement acceptance questions.
Company and rehabilitation focus
Tyromotion develops robotic and sensor-based rehabilitation equipment. Its official contact page identifies Tyromotion GmbH in Graz, Austria, and Tyromotion Inc. in the United States. Buyers should establish the local contracting and service organization, then select devices around the rehabilitation activities their clinical team intends to provide.
Amadeo for hand and finger training
The Amadeo page describes robot-assisted finger and hand rehabilitation for patients with motor dysfunction affecting the distal upper extremity. It includes assessment and training functions, with an EMG module discussed in the product material. Confirm the included modules and accessories in the quotation rather than assuming every illustrated function is standard equipment.
Lexo for gait rehabilitation
The Lexo page describes an end-effector gait trainer using motorized footplates, with body and trunk support. This differs mechanically from a wearable leg exoskeleton. Evaluation should address patient transfer, positioning, therapist access and the configuration needed for the intended population. The device's current instructions for use should determine detailed indications, contraindications and fitting limits.
A specific European regulatory statement
In a December 3, 2025 announcement, Tyromotion reported EU MDR Class IIa certification for Lexo, Omego, Diego, Amadeo and tyroS. The dated list supports a model-specific European regulatory account. It should not be expanded to every product, accessory, software version or non-European market. Obtain the applicable certificate, declaration and labeling for the configuration under consideration.
Software and information flow
The company's current FAQ distinguishes tyroS, used to set up and adapt sessions at devices, from Maya, used for patient documentation, reporting and utilization information. It describes Maya data as stored on the clinic's premises. Procurement should still define access permissions, backups, exports and integration responsibilities for the proposed installation.
Ask the supplier to document supported connectivity and remote support methods. Network access should follow the manufacturer's device guidance and the institution's IT process, with named responsibility for configuration and updates.
Clinical implementation and evidence
A trial should cover the full appointment cycle, including preparation, transfer, fitting, supervised training, documentation and cleaning. Measure operational performance separately from clinical outcomes. Patient stories and supplier summaries can identify questions to investigate, but they are not guarantees of recovery or evidence that every patient will benefit.
Define therapist training, competency checks and escalation arrangements before routine use. Compare the proposed device mix with the facility's clinical objectives and available staff rather than treating a large equipment package as automatically more effective.
Regional service and purchasing
Tyromotion's FAQ distinguishes direct service arrangements in the DACH region and United States from support through authorized local partners elsewhere. Request written confirmation of the partner, maintenance intervals, parts supply and service response for the purchasing country. Specify the device, software version and intended installation site when seeking a proposal.
Questions before committing
Which patient groups and tasks fall within the local device labeling?
Which robotic, sensor and software modules are included?
Who manages training, maintenance, patient data and software updates?
What observable requirements determine successful commissioning?
Explore Medical and Rehabilitation Robots, Write a Robotics Buyer Brief, or Robotics RFQ.