MyoPro 2x
By Myomo
Custom-fitted powered myoelectric upper-limb orthosis prescribed and supplied through qualified providers after clinical evaluation.
Product Overview
MyoPro 2x is a custom-fitted powered myoelectric upper-limb orthosis for adolescents and adults with long-term muscle weakness or partial paralysis. It senses remaining EMG activity to assist elbow movement and, depending on configuration, wrist and hand function. A qualified orthotics and prosthetics provider assesses fit and clinical suitability through a prescription-based access pathway.
Next step: Review Myomo’s patient evaluation and access process and discuss suitability with a qualified clinician or O&P provider.
Positioning & Buyer Fit
Custom-fitted powered myoelectric orthosis supporting prescribed elbow and configuration-dependent hand function for people with long-term upper-limb weakness or partial paralysis.
Patients and clinicians evaluating a custom prescription orthosis through a qualified orthotics and prosthetics provider and an individual clinical and payer review.
Use Case & Product Classification
Powered myoelectric upper-limb orthosis
- Weight: 3–4 lb (1.4–1.8 kg) depending on custom components
- Battery: interchangeable 10.8 V 3350 mAh 36.2 Wh lithium-ion
- Battery use: manufacturer describes a full day of typical functional use
- Fit: custom made for left or right arm after provider evaluation
- Assistance: powered elbow and configuration-dependent hand support
- Maximum elbow lifting assistance: 5 lb
- Ingress protection: IP21
- Indication: adolescents and adults with long-term muscle weakness or partial paralysis per manufacturer IFU
- US regulatory wording: FDA-listed Class II and 510(k)-exempt per Myomo
Claims & Evidence
Myomo reports a typical device weight of 3–4 lb depending on custom components and describes the battery as designed for a full day of typical functional use. The manufacturer user manual specifies up to 5 lb of elbow lifting assistance and IP21.
Certification & Regulatory Notes
FDA-listed Class II and 510(k)-exempt in the United States per Myomo; not 510(k)-cleared.
Myomo’s current 2x user manual describes the device as prescription-only and for use under provider supervision or after provider instruction. Clinical eligibility, fit, and payer authorization are individual determinations.
Pricing & Commercial Access
No official public price found
Pricing Not Public
Unknown
Not specified
Unknown
02/10/2026
Tell us about your task, users, industry and region. We can help identify relevant products, suppliers and practical next steps.