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Center For Pain and Stress Research Ltd

US

Last updated May 31, 2026

Part of Center For Pain And Stress Research, Ltd.

What Center For Pain and Stress Research Ltd makes

Center for Pain and Stress Research Ltd manufactures transcutaneous electrical nerve stimulation (TENS) systems designed for pain relief, including the Dolphin Neurostim device. These systems deliver low-voltage electrical currents through electrodes placed on the skin to modulate pain signals.

The company’s products are classified as Class II devices 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 Center For Pain and Stress Research Ltd manufacture?

Center For Pain and Stress Research Ltd specializes in analgesic transcutaneous electrical nerve stimulation (TENS) systems, which are designed to provide pain relief. These devices work by delivering low-voltage electrical currents through electrodes placed on the skin to interfere with pain signals. The most common example is the Dolphin Neurostim, a TENS system developed for managing pain.

Where is Center For Pain and Stress Research Ltd based?

The company is headquartered in the United States. This location is relevant for regulatory compliance, as their devices are subject to FDA oversight and classification.

How are the company’s devices classified under FDA regulations?

The devices manufactured by Center For Pain and Stress Research Ltd are classified as Class II under FDA regulations. This classification applies to devices that generally pose moderate risk and require special controls to ensure safety and effectiveness, such as TENS systems, which require validation of their electrical safety and clinical performance.

Are the company’s devices listed in any regulatory registries?

Yes, the company’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers, regulators, and patients to verify device details, such as manufacturer information, model names, and regulatory status.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
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Phone
1-800-567-7246
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
251050084

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
Dolphin Neurostim Classic
FDA UDI
Class IIActive
Dolphin Neurostim Professional
FDA UDI
Class IIActive

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