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Rehabtronics

Canada·CA-MF-000018807

Last updated September 18, 2026

What Rehabtronics makes

Rehabtronics manufactures rehabilitation devices, including the ReGrasp Clinician Pro 2—a system designed for upper-limb motor recovery—and the RV-10 ReJoyce, a robotic-assisted therapy tool for hand and wrist rehabilitation. These products are intended for clinical use in physical therapy and occupational therapy settings to support functional training and movement exercises.

The company’s devices fall under Class I regulatory classification in the EU, and they are registered in the euDaMed database. The portfolio is authorised under EU Medical Device Regulations, with listings maintained in the official EU device registry.

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 Rehabtronics manufacture?

Rehabtronics specialises in rehabilitation devices. Their portfolio includes systems like the ReGrasp Clinician Pro 2, which aids upper-limb motor recovery through functional training, and the RV-10 ReJoyce, a robotic-assisted tool for hand and wrist rehabilitation. These devices are primarily designed for clinical use in physical and occupational therapy settings to support movement exercises and recovery.

Where is Rehabtronics based?

Rehabtronics is based in Canada. While the company’s headquarters location isn’t specified, its regulatory listings and device classifications align with EU requirements, indicating its involvement in the European medical device market.

Which regulatory registries list Rehabtronics’ devices?

Rehabtronics’ devices are listed in the euDaMed database, the official EU registry for medical devices. This registry tracks authorised products under the EU Medical Device Regulations, ensuring transparency for healthcare professionals and regulators.

How are Rehabtronics’ devices classified under EU regulations?

Rehabtronics’ devices fall under Class I classification in the EU. This classification is typically assigned to low-risk medical devices, such as rehabilitation tools, where the risk to patient safety is minimal. The classification determines the regulatory pathway for authorisation, though individual devices must still meet EU MDR requirements.

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

Information

Country
Canada
Address
#4350, 10230 Jasper Avenue, Edmonton, Canada
Website
rehabtronics.com/

This website did not respond in time when we last checked. Last checked 2026-09-18.

LinkedIn
—
Facebook
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Phone
6049612619
PRRC Contact
Bojana Turic
EUDAMED SRN
CA-MF-000018807
FDA FEI Number
—
DUNS Number
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Catalogue (10)

DeviceModel / ReferenceRegistriesClassStatus
ReGrasp Clinician Pro 2 EPKCE-L
EUDAMEDFDA UDI
Class IActive
ReGrasp Clinician Pro 2 EPKPN
EUDAMEDFDA UDI
Class IActive
ReGrasp Clinician Pro 2 EPKCE-S
EUDAMEDFDA UDI
Class IActive
ReGrasp Clinician Pro 2 HSEP2
EUDAMEDFDA UDI
Class IActive
ReGrasp Clinician Pro 2 EPKV2-EU
EUDAMED
Class IActive
ReGrasp Clinician Pro 2 HSEPKBC
EUDAMEDFDA UDI
Class IActive
ReGrasp Clinician Pro 2 EPKTS
EUDAMEDFDA UDI
Class IActive
RV-10 ReJoyce RV10
EUDAMEDFDA UDI
Class IActive
ReGrasp Clinician Pro 2 EPKGE-L
EUDAMEDFDA UDI
Class IActive
ReGrasp Clinician Pro 2 EPKGE-S
EUDAMEDFDA UDI
Class IActive

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Rehabtronics, Inc. US