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MAGIC RACE LLC

US

Last updated May 30, 2026

What MAGIC RACE LLC makes

Magic Race LLC manufactures line-powered transcutaneous electrical stimulation (TENS) systems designed for physical therapy applications. Their devices include models like NeoTone and NeoControl, which are intended for neuromuscular stimulation and pain management.

These products fall under FDA Class II regulation and are 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 Magic Race LLC manufacture?

Magic Race LLC specializes in line-powered transcutaneous electrical stimulation (TENS) systems tailored for physical therapy. These devices are designed to deliver neuromuscular stimulation and assist in pain management. The most common category is the physical therapy TENS system, with examples including models like NeoTone and NeoControl.

Where is Magic Race LLC based?

Magic Race LLC is headquartered in the United States. The company’s location is relevant for understanding regulatory frameworks, as it operates under U.S. medical device regulations.

Which regulatory registries list Magic Race LLC’s devices?

Magic Race LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and compliance tracking for Class II devices, which include their TENS systems like NeoTone and NeoControl.

How are Magic Race LLC’s devices classified by regulatory authorities?

Magic Race LLC’s devices fall under FDA Class II classification. This classification is assigned based on the risk level of the product—Class II devices generally pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
(498) 934-1040
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
080456235

Catalogue (7)

DeviceModel / ReferenceRegistriesClassStatus
NeoTone N-0242-T
FDA UDI
Class IIActive
NeoTone N-0243-B-110VAC
FDA UDI
Class IIActive
NeoControl N-0228-F-220VAC
FDA UDI
Class IIActive
NeoControl N-0228-G-110VAC
FDA UDI
Class IIActive
NeoTone N-0242-B
FDA UDI
Class IIActive
NeoTone N-0243-B-220VAC
FDA UDI
Class IIActive
NeoControl N-0227-A
FDA UDI
Class IIActive

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