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Deployment

Myomo MyoPro at North America

Powered (motor-actuated) upper-limb orthosis controlled by the user's own EMG (myoelectric) muscle signals: faint bicep/tricep signals trigger powered elbow/hand assistance for people with arm paralysis. FDA 510(k) cleared (K062631). Powered, user-EMG-controlled.

Myomo MyoPro by Myomo · Catalog entry · 1 source · not yet field-verified


Machine-readable surfaces

North American operational deployment. Myomo MyoPro operations.

Trust tier
Catalog entry · 1 source · not yet field-verified
Last updated
2026-06-08
Model
Myomo MyoPro
Company
Myomo
Location
North America
Status
operational
ID
49e66fb0-e16d-4801-8371-c9c836fe7ac7

Sources (1)

  1. https://rover.report
Methodology: Verified · 1 source (no primary) · last reviewed 2026-06-08

Verification posture

Verified

Low confidence

Review state

Stable

Last reviewed 2026-06-08

Maturity + lifecycle

Maturity stage: commercial

Lifecycle: active

Architectural position

Cohort: exoskeleton

Sources by quality tier

1
unclassified
Unclassified source

The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.

Methodology surface for Myomo MyoPro at North America.

Common questions

What is the Myomo MyoPro deployment at North America?
Myomo MyoPro, built by Myomo, is recorded as a deployment at North America on the DEPLOY registry. Myomo operates the deployment directly.
Who operates Myomo MyoPro at North America?
Myomo, the manufacturer of Myomo MyoPro, operates this deployment directly. This is a maker-deploys-its-own-product arrangement rather than a customer pilot.
Have there been incidents at the Myomo MyoPro deployment at North America?
No active incidents affecting this deployment are recorded on the DEPLOY registry. Absence of recorded incidents is not a guarantee no incident occurred; DEPLOY records only sourced incidents and suppresses retracted ones.

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