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WELLNESS WITHOUT LIMITS LLC

US

Last updated May 24, 2026

What WELLNESS WITHOUT LIMITS LLC makes

Wellness Without Limits LLC manufactures phototherapy devices, including red and infrared light units, blue-light lamps designed for home use, and handheld electromagnetic stimulators for deep-tissue treatment. Their portfolio also includes combined red/blue light phototherapy units, primarily intended for therapeutic applications.

All devices are classified as Class II under FDA regulations 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 Wellness Without Limits LLC manufacture?

Wellness Without Limits LLC specializes in phototherapy devices, including red and infrared light therapy units, blue-light lamps designed for home use, and handheld deep-tissue electromagnetic stimulators. They also produce combined red/blue light phototherapy units, all intended for therapeutic applications.

Where is Wellness Without Limits LLC based?

The company is based in the United States, as indicated in its regulatory documentation.

Which regulatory registries list Wellness Without Limits LLC’s devices?

Wellness Without Limits LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database, which is a central registry for tracking medical devices authorized in the United States.

How are Wellness Without Limits LLC’s devices classified under FDA regulations?

All devices manufactured by Wellness Without Limits LLC fall under Class II classification according to FDA regulations. This classification typically applies to devices that 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
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Website
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LinkedIn
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Facebook
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Email
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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
020287489

Catalogue (21)

DeviceModel / ReferenceRegistriesClassStatus
LS Pro Systems PB-MXP100
FDA UDI
Class IIActive
LS Pro Systems XP6
FDA UDI
Class IIActive
LS Pro Systems XL200-SI
FDA UDI
Class IIActive
LS Pro Systems XP1
FDA UDI
Class IIActive
LS Pro Systems XP3
FDA UDI
Class IIActive
LS Pro Systems H155
FDA UDI
Class IIActive
LS Pro Systems B112
FDA UDI
Class IIActive
LS Pro Systems PB-MXP171
FDA UDI
Class IIActive
LS Pro Systems F104
FDA UDI
Class IIActive
LS Pro Systems LB114-SI
FDA UDI
Class IIActive
LS Pro Systems XL200
FDA UDI
Class IIActive
LS Pro Systems G264B
FDA UDI
Class IIActive
LS Pro Systems L132
FDA UDI
Class IIActive
LS Pro Systems UB128-SI
FDA UDI
Class IIActive
LS Pro Systems T90
FDA UDI
Class IIActive
LS Pro Systems DSD120
FDA UDI
Class IIActive
LS Pro Systems G264-SI
FDA UDI
Class IIActive
LS Pro Systems G264
FDA UDI
Class IIActive
LS Pro Systems L132B
FDA UDI
Class IIActive
LS Pro Systems F122-SI
FDA UDI
Class IIActive
LS Pro Systems H155-SI
FDA UDI
Class IIActive

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