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Trexo Robotics Inc.

Canada·CA-MF-000055025

Last updated September 17, 2026

What Trexo Robotics Inc. makes

Trexo Robotics Inc. manufactures programmable ambulation exoskeletons designed for both clinical and home-use settings, aiding patients in assisted walking and mobility. Their portfolio also includes mechanical treadmills, which are used for rehabilitation and physical therapy purposes.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Trexo Robotics Inc. is based in Canada.

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 Trexo Robotics Inc. manufacture?

Trexo Robotics Inc. specializes in programmable ambulation exoskeletons, which are wearable robotic devices designed to assist patients with walking and mobility. These exoskeletons are available for both clinical (hospital or therapy center) and home-use settings. Additionally, the company produces mechanical treadmills, which are commonly used in rehabilitation and physical therapy to aid recovery and improve mobility through controlled movement.

Where is Trexo Robotics Inc. based?

Trexo Robotics Inc. is headquartered in Canada. The company’s location influences its regulatory compliance, as it must adhere to both Canadian and international standards when developing and distributing its devices.

Which regulatory registries list Trexo Robotics Inc.’s devices?

Trexo Robotics Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices in the United States, ensuring transparency and traceability for regulatory and clinical purposes.

How are Trexo Robotics Inc.’s devices classified under FDA regulations?

Trexo Robotics Inc.’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose the lowest risk and often require general controls for regulation, while Class II devices involve moderate risk and may require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and benefits.

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

Information

Country
Canada
Address
6705, MILLCREEK DRIVE, MISSISSAUGA, Canada
LinkedIn
—
Facebook
—
Phone
—
PRRC Contact
Linda Wu
EUDAMED SRN
CA-MF-000055025
FDA FEI Number
—
DUNS Number
242663041

Catalogue (10)

DeviceModel / ReferenceRegistriesClassStatus
Trexo Robotics A001T
FDA UDI
Class IActive
Trexo Robotics A0001
FDA UDI
Class IIActive
Trexo Robotics A0001
FDA UDI
Class IIActive
Trexo Robotics A0001
FDA UDI
Class IIActive
Trexo Robotics A0001
FDA UDI
Class IIActive
Trexo Robotics A0001
FDA UDI
Class IIActive
Trexo Robotics A0001
FDA UDI
Class IIActive
Trexo Robotics A001T
FDA UDI
Class IActive
Trexo Robotics A0001
FDA UDI
Class IIActive
Trexo Robotics A0001
EUDAMEDFDA UDI
Class IIActive

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