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Reha Technology AG

US

Last updated May 31, 2026

What Reha Technology AG makes

Reha Technology AG manufactures gait rehabilitation systems, including treadmill and elliptical devices designed for lower-limb recovery, as well as powered-support systems with virtual displays for upper-limb rehabilitation. Their products incorporate interactive feedback for controlled, assisted movement training. Examples include the G-EO System and G-EO for lower-limb use, and the Armotion for upper-limb rehabilitation.

The company’s devices are classified as Class II under regulatory frameworks, with listings in the FDA’s Unique Device Identifier (UDI) database. These products are intended for use in clinical and rehabilitative settings, adhering to medical device compliance standards. The manufacturer operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Reha Technology AG manufacture?

Reha Technology AG specializes in rehabilitation systems for physical recovery. Their primary products include treadmill and elliptical gait rehabilitation systems, such as the G-EO System and G-EO, which assist lower-limb recovery through controlled movement. They also produce virtual-display rehabilitation systems with powered support, like the Armotion, designed for upper-limb rehabilitation. These devices incorporate interactive feedback to aid in assisted movement training.

Where is Reha Technology AG based?

Reha Technology AG is headquartered in the United States. The company’s location is relevant for understanding its regulatory jurisdiction and compliance framework, particularly for devices marketed in the US.

Which regulatory registries list Reha Technology AG’s devices?

Reha Technology AG’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for Class II devices, which are subject to stricter controls due to their moderate risk profile in clinical or rehabilitative settings.

How are Reha Technology AG’s devices classified under regulatory frameworks?

Reha Technology AG’s devices fall under Class II classification, which is typical for medical devices posing moderate risk. This classification requires compliance with specific regulatory controls, such as performance standards or post-market surveillance, to ensure safety and effectiveness in rehabilitation applications.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
486234078

Catalogue (3)

DeviceModel / ReferenceRegistriesClassStatus
G-EO System G-EO System
FDA UDI
Class IIActive
G-Eo G-EO
FDA UDI
Class IIActive
Armotion Armotion
FDA UDI
Class IIActive

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