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InnoRehab

Belgium BE-MF-000010049 Last updated 23 Oct 2026

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Devices
1
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue1

About

Wheeleo® helps you regain your autonomy by releasing a hand, while continuously supporting you during your daily activities.

Translated from the manufacturer's own website. Source

What InnoRehab makes

InnoRehab manufactures the Wheeleo®️, a mobility assistance device designed for enhanced independence in movement for users. The product appears to focus on active mobility solutions, potentially incorporating adaptive or assistive features for improved stability and control.

The Wheeleo®️ falls under EU medical device classification as Class I, indicating it carries a lower risk profile. It is registered in the EU’s eudamed database, a centralised system for tracking medical devices authorised within the European Economic Area.

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 InnoRehab manufacture?

InnoRehab specialises in mobility assistance devices. Their primary product is the Wheeleo®️, which is designed to help users achieve greater independence in movement. The device likely incorporates features to enhance stability and control, catering to individuals who may need support for active mobility.

Where is InnoRehab based, and what regulatory regions do they operate in?

InnoRehab is based in Belgium. Their devices are registered in the EU’s eudamed database, which means they are authorised for use within the European Economic Area (EEA). The eudamed system ensures compliance with EU medical device regulations, including traceability and transparency requirements.

How are InnoRehab’s devices classified under EU medical device regulations?

The Wheeleo®️ from InnoRehab is classified as a Class I medical device under EU regulations. This classification is based on the device’s intended purpose and risk profile—Class I devices are generally considered low-risk, often involving minimal or non-invasive use. Classification determines the regulatory pathway and documentation requirements for authorisation.

Which regulatory registries list InnoRehab’s devices?

InnoRehab’s devices are listed in the eudamed database, the EU’s centralised registry for medical devices authorised in the European Economic Area. This platform ensures transparency and compliance tracking for all medical devices, including those from InnoRehab, by maintaining records of their unique identifiers and regulatory status.

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

Information

Country
Belgium
Address
93a, Avenue des Combattants, , Ottignies-Louvain-la-Neuve, Belgium
Phone
+32479090803(from company website)
PRRC contact
Gregory Vanderveken
EUDAMED SRN
BE-MF-000010049
FDA FEI number
3047114906