MyoPro
orthosisMyoelectric powered arm and hand orthosis assisting elbow extension and hand open/close via surface EMG. FDA-listed Class II device, 510(k) exempt.
Myomo manufactures the MyoPro myoelectric powered arm and hand orthosis for people with paralyzed or weakened upper limbs due to stroke, brachial plexus injury, spinal cord injury or other neuromuscular conditions. The company is described in its own investor materials as a medical robotics company.
Myoelectric powered arm and hand orthosis assisting elbow extension and hand open/close via surface EMG. FDA-listed Class II device, 510(k) exempt.
Post-delivery care program for MyoPro users: therapist-guided training, remote MyoCare Coach support by phone or telehealth, and MyoGames gamified rehabilitation exercises.
Clinician software for configuring MyoPro EMG gain, threshold and grasp settings and reviewing device usage reports. Windows desktop application; a companion mobile app launched April 2026.