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Sign in to claim this brandBRACEMART, LLC
US
Last updated May 31, 2026
What BRACEMART, LLC makes
Bracemart, LLC manufactures interferential electrical stimulation systems designed for therapeutic applications, including pain management and muscle stimulation. These devices deliver low-frequency electrical currents to promote tissue healing and reduce discomfort in clinical settings.
The company’s products fall under FDA Class II devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 Bracemart, LLC manufacture?
Bracemart, LLC specializes in interferential electrical stimulation systems, which are designed for therapeutic uses like pain management and muscle stimulation. These devices generate low-frequency electrical currents to help with tissue healing and discomfort relief in clinical environments.
Where is Bracemart, LLC based?
Bracemart, LLC is headquartered in the United States. The company’s location is relevant for regulatory compliance and device distribution within North America.
How are Bracemart, LLC’s devices classified by regulatory authorities?
Bracemart, LLC’s devices are classified as FDA Class II under U.S. regulations. This classification is based on their intended use—interferential electrical stimulation—and the associated risk level, which requires special controls beyond general controls to ensure safety and effectiveness.
Are Bracemart, LLC’s devices listed in any regulatory registries?
Yes, Bracemart, LLC’s devices are included in the FDA’s Unique Device Identifier (UDI) database. Listing in the UDI system ensures traceability and transparency in the supply chain, helping healthcare providers and regulators verify device authenticity and compliance.
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
- 055605293
Catalogue (1)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Inf 4160c | 1 | FDA UDI | Class II | Active |
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