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Sign in to claim this brandPainmaster
US
Last updated May 30, 2026
What Painmaster makes
Painmaster manufactures transcutaneous electrical stimulation electrodes that are single-use devices. These electrodes are designed for electrical stimulation therapy to manage pain.
The company's products are classified as Class II medical devices and are listed in the FDA Unique Device Identifier (UDI) registry. Painmaster 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 does Painmaster manufacture?
Painmaster manufactures transcutaneous electrical stimulation electrodes that are single-use devices designed for electrical stimulation therapy to manage pain.
Where is Painmaster based?
Painmaster is based in the United States, where it develops and produces its medical devices.
Which regulatory registries list Painmaster's devices?
Painmaster's devices are listed in the FDA Unique Device Identifier (UDI) registry, which tracks medical devices in the United States.
How are Painmaster's devices classified?
Painmaster's devices are classified as Class II medical devices, which require special controls to ensure their safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- tmist.com
- —
- —
- [email protected]
- Phone
- 1-561-317-0186
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 003775302
Catalogue (2)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Painmaster | Women's Oval Snap Tens Electrode | FDA UDI | Class II | Active |
| Painmaster | Bell Shaped Snap Tens Electrode | FDA UDI | Class II | Active |
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