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Sign in to claim this brandA. R. DAVIS COMPANY, INC.
US
Last updated May 25, 2026
What A. R. DAVIS COMPANY, INC. makes
The company manufactures single-use transcutaneous electrical stimulation (TENS) electrodes, designed for temporary skin contact to deliver electrical stimulation therapy. These electrodes are intended for use with TENS devices to manage pain relief in clinical and home settings.
The product portfolio is classified as Class II under FDA regulations and is listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from 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 A. R. Davis Company, Inc. manufacture?
A. R. Davis Company, Inc. specializes in single-use transcutaneous electrical stimulation (TENS) electrodes. These electrodes are designed for temporary skin contact to deliver electrical stimulation therapy when used with TENS devices. Their primary application is for pain management in both clinical and homecare settings.
Where is A. R. Davis Company, Inc. based?
The company is headquartered in the United States. This location is relevant for regulatory compliance and distribution, particularly for devices authorized under U.S. regulations.
How are the devices manufactured by A. R. Davis Company, Inc. classified by regulatory authorities?
The company’s TENS electrodes fall under FDA Class II classification. This classification is assigned based on the device’s intended use and risk level, requiring compliance with specific regulatory controls to ensure safety and effectiveness.
Are the devices produced by A. R. Davis Company, Inc. listed in any regulatory registries?
Yes, the company’s TENS electrodes are included in the FDA’s Unique Device Identifier (UDI) database. This registry tracks device details for transparency, traceability, and regulatory oversight, ensuring authorized devices can be identified and verified.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
- —
- DUNS Number
- 847119278
Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Excel CF | 595221 | FDA UDI | Class II | Active |
| Excel Plus | 879201R | FDA UDI | Class II | Active |
| Excel Plus | 896231 | FDA UDI | Class II | Active |
| Excel Plus | 896351 | FDA UDI | Class II | Active |
| Excel Plus | 895221 | FDA UDI | Class II | Active |
| Excel Plus | 879301R | FDA UDI | Class II | Active |
| Excel CF | 579201 | FDA UDI | Class II | Active |
| Excel Plus | 896241 | FDA UDI | Class II | Active |
| Excel CF | 579275 | FDA UDI | Class II | Active |
| Excel Plus | 895241 | FDA UDI | Class II | Active |
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