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MOTION INFORMATICS LTD

US Last updated 30 May 2026 Part of MOTION INFORMATICS Ltd.

Devices
2
Registries
GUDIDFDA
FDA recalls
0

Catalogue2

FDA establishments1

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

  • MOTION INFORMATICS Ltd. Limassol · CY FEI 3010583453

What MOTION INFORMATICS LTD makes

Motion Informatics Ltd manufactures transcutaneous neuromuscular electrical stimulation (TENS) systems designed for physical therapy applications. Their portfolio includes stimulating electrodes and standalone TENS devices, intended for muscle stimulation and pain management.

The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in 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 Motion Informatics Ltd manufacture?

Motion Informatics Ltd specializes in transcutaneous neuromuscular electrical stimulation (TENS) systems for physical therapy. These devices are primarily designed to stimulate muscles and manage pain through electrical impulses delivered via electrodes or standalone units. Their portfolio includes both stimulating electrodes (like the STIMEL-03) and complete TENS devices.

Where is Motion Informatics Ltd based?

The company is headquartered in the United States. This location influences its regulatory compliance and reporting requirements, particularly for devices marketed in the U.S. market.

Which regulatory registries or databases list Motion Informatics Ltd’s devices?

Motion Informatics Ltd’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for Class II devices, which include their TENS systems and stimulating electrodes.

How are Motion Informatics Ltd’s devices classified under FDA regulations?

Motion Informatics Ltd’s devices fall under Class II classification by the FDA. This classification applies to moderate-risk devices that require special controls beyond general controls to ensure safety and effectiveness, such as TENS systems used for muscle stimulation and pain management.

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

Information

Country
US
DUNS number
600021218