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Sign in to claim this brandHi-Dow International Incorporated
US
Last updated May 25, 2026
What Hi-Dow International Incorporated makes
Hi-Dow International Incorporated manufactures transcutaneous electrical nerve stimulation (TENS) systems for pain management, including both analgesic and physical therapy neuromuscular stimulation devices. Their portfolio also includes disposable and reusable transcutaneous electrical stimulation electrodes, as well as home-use short-wave diathermy systems for therapeutic treatment.
All listed devices fall under Class II regulation and are registered 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 Hi-Dow International Incorporated manufacture?
Hi-Dow International Incorporated specializes in transcutaneous electrical stimulation (TENS) devices. Their portfolio includes analgesic TENS systems designed for pain management, physical therapy neuromuscular electrical stimulation systems for muscle rehabilitation, and transcutaneous electrical stimulation leads and electrodes (both single-use and reusable). Additionally, they produce home-use short-wave diathermy systems for therapeutic treatments. These devices are primarily focused on non-invasive electrical and thermal therapies.
Where is Hi-Dow International Incorporated based?
Hi-Dow International Incorporated is headquartered in the United States. The company’s location is relevant for regulatory compliance and device registration purposes, particularly in markets like the U.S., where manufacturers must adhere to local regulatory requirements.
Which regulatory registries list Hi-Dow International Incorporated’s devices?
Hi-Dow International Incorporated’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is used to track medical devices throughout their lifecycle, ensuring traceability and compliance with regulatory standards. This registry is particularly important for transparency in the medical device supply chain.
How are Hi-Dow International Incorporated’s devices classified under medical device regulations?
All of Hi-Dow International Incorporated’s listed devices fall under Class II classification. Class II devices are generally considered to pose moderate risk and require special controls to ensure their safety and effectiveness, such as performance standards, post-market surveillance, or labeling requirements. This classification applies to their TENS systems, electrodes, and diathermy devices.
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
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- DUNS Number
- 124034476
Catalogue (58)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| TrueStim | HD-08D(TSG-D1) | FDA UDI | Class II | Active |
| TenStim | JQ-5C-S-12 | FDA UDI | Class II | Active |
| HiDow, TrueStim | JQ-5C-N-RECEIVER | FDA UDI | Class II | Active |
| HiDow | HD-09C | FDA UDI | Class II | Active |
| HiDow | HD-09E | FDA UDI | Class II | Active |
| HiDow | JQ-5C-S | FDA UDI | Class II | Active |
| HiDow | JQ-5C-S | FDA UDI | Class II | Active |
| HiDow | HD-09H | FDA UDI | Class II | Active |
| PainPod | JQ-5C-M | FDA UDI | Class II | Unknown |
| HiDow | JQ-5C-S | FDA UDI | Class II | Active |
| HiDow | AcuGloves(HD-09A) | FDA UDI | Class II | Active |
| HiDow | JQ-5C-Y | FDA UDI | Class II | Active |
| HiDow | HD-19A | FDA UDI | Class II | Active |
| TrueStim | JQ-5C-Y | FDA UDI | Class II | Active |
| TrueStim | HD-08B(TSG-B1) | FDA UDI | Class II | Active |
| Echo | JQ-5C-R | FDA UDI | Class II | Active |
| HiDow | HD-09F | FDA UDI | Class II | Active |
| HiDow | WR-2605 | FDA UDI | Class II | Active |
| TrueStim | HD-08B(TSG-E1) | FDA UDI | Class II | Active |
| HiDow | JQ-5C-R | FDA UDI | Class II | Active |
| PainPod | JQ-5C-B | FDA UDI | Class II | Active |
| TrueStim | HD-08A(TSG-A1) | FDA UDI | Class II | Active |
| HiDow | JQ-5C-E | FDA UDI | Class II | Active |
| TrueStim | HD-08C(TSG-C1) | FDA UDI | Class II | Active |
| HiDow | JQ-5C-S | FDA UDI | Class II | Active |
| PainPod | JQ-5C-07A | FDA UDI | Class II | Active |
| Somacare | JQ-5C-C | FDA UDI | Class II | Active |
| HiDow | HD-09K | FDA UDI | Class II | Active |
| HiDow | HD-5N-Y | FDA UDI | Class II | Active |
| HiDow | HD-09D | FDA UDI | Class II | Active |
| HiDow | JQ-5C-C | FDA UDI | Class II | Active |
| HiDow | JQ-5C-R | FDA UDI | Class II | Active |
| Hidow SuperTens | JQ-5C-W | FDA UDI | Class II | Active |
| TrueStim | JQ-5C-J | FDA UDI | Class II | Active |
| HiDow | JQ-5C-R | FDA UDI | Class II | Active |
| PainPod | JQ-5C-M | FDA UDI | Class II | Active |
| HiDow | JQ-5C-R | FDA UDI | Class II | Active |
| HiDow | JQ-5C-S | FDA UDI | Class II | Active |
| TenStim | JQ-5C-R | FDA UDI | Class II | Active |
| HiDow | JQ-5C-Y-RECEIVER | FDA UDI | Class II | Active |
| HiDow TrueStim | HD-5N-Y | FDA UDI | Class II | Active |
| Hi-Dow Pro-Tech | HD-5N-N-Receiver | FDA UDI | Class II | Active |
| HiDow | HD-09B | FDA UDI | Class II | Active |
| Pro-Tech | JQ-5C-C | FDA UDI | Class II | Active |
| HiDow | JQ-5C-S | FDA UDI | Class II | Active |
| Myopux | HD-5N-20A-RECEIVER | FDA UDI | Class II | Active |
| COPPER Fit | JQ-5C-07A | FDA UDI | Class II | Active |
| Namirsa | JQ-5C-R | FDA UDI | Class II | Active |
| Pro-Tech | HD-5N-N | FDA UDI | Class II | Active |
| HiDow | JQ-5C-R | FDA UDI | Class II | Active |
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