Strong Commitment to Safety, Stability, and Long-Term Partnership

We are pleased to announce an important milestone in the ongoing development of our high-quality rehabilitation solutions:

Our devices – Lexo, Omego, Diego, Amadeo, and tyroS – have been successfully certified as Class IIa medical devices under the EU Medical Device Regulation (MDR).

This certification officially confirms that all our products now meet the stringent MDR requirements for safety, performance, and clinical evidence. It serves as clear proof of our team’s expertise – and demonstrates our commitment to the highest standards, ensuring that Tyromotion is fully prepared for the demanding regulatory landscape in Europe.

At a time when regulations are becoming increasingly complex and requirements continuously grow, MDR certification provides one essential advantage: reliable security for you and your customers.

What MDR certification means:

  • Maximum safety and sales stability – all our devices comply with current MDR requirements.
  • Strong arguments for tenders and proposals – backed by up-to-date and robust regulatory documentation.
  • Long-term investment security for hospitals, clinics, and therapy centers.
  • A partnership built on equality – with a manufacturer that consistently prioritizes innovation, quality, and regulatory excellence.

The MDR certification is more than a procedural milestone for us. It forms the foundation upon which we will continue to develop future-ready, safe, and reliable rehabilitation technology you and your patients can trust – today, tomorrow, and for many years to come.

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