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Sign in to claim this brandHI-DOW INTERNATIONAL INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 2555 Metro Blvd, Maryland Heights, MO, 63043
- Website
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- Phone
- —
- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
- 3003895865
- DUNS Number
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Catalogue (22)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Pain Remedy | C05W | FDA UDI | Class II | Unknown |
| HiDow | JQ-5C-C | FDA UDI | Class II | Active |
| HiDow | JQ-5C-N | FDA UDI | Class II | Active |
| HiDow | JQ-5C-N | FDA UDI | Class II | Active |
| Hi-Dow | HD-5N-N | FDA UDI | Class II | Active |
| Core | HD-5N-F | FDA UDI | Class II | Unknown |
| Myopux | HD-5N-20A | FDA UDI | Class II | Active |
| TrueStim | HD-5N-Y | FDA UDI | Class II | Active |
| Echo | JQ-5C-D | FDA UDI | Class II | Active |
| HiDow | JQ-5C-R | FDA UDI | Class II | Active |
| HiDow | JQ-5C-R | FDA UDI | Class II | Active |
| TrueStim | JQ-5C-J | FDA UDI | Class II | Active |
| HiDow, SuperTens | JQ-5C-W | FDA UDI | Class II | Active |
| Hi-Dow | JQ-5C-T | FDA UDI | Class II | Active |
| PainPod | JQ-5C-C | FDA UDI | Class II | Unknown |
| HiDow | HD-09J | FDA UDI | Class II | Active |
| Hi-Dow Wireless TENS/EMS System (Model HD-5N) | K163393 | FDA 510(k) | Class II | Active |
| Wrap Accessory Electrodes | K210383 | FDA 510(k) | Class II | Active |
| Wrap accessory electrodes | K190617 | FDA 510(k) | Class II | Active |
| Hi-Dow PRO TOUCH WIRELESS 6-12 (HD-19A) | K233461 | FDA 510(k) | Class II | Active |
| Hi-Dow-Xp | K102598 | FDA 510(k) | Class II | Active |
| Pulsed electromagnetic field wrap | K202337 | FDA 510(k) | Class II | Active |
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