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Vielight Inc

US

Last updated May 23, 2026

What Vielight Inc makes

Vielight Inc manufactures red and infrared light phototherapy units designed for therapeutic applications. Their devices, such as the Vielight Relief, are intended for non-invasive treatment using specific wavelengths of light to target conditions like pain or inflammation.

The company’s products fall under Class II regulatory classification in the United States and are listed in the FDA’s Unique Device Identifier (UDI) database. Vielight Inc operates from the US, adhering to domestic medical device regulations.

Written from this company's registered devices by an AI model, 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
202888269

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
Vielight Relief RLF
FDA UDI
Class IIUnknown
Vielight Relief RLF
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Vielight Inc Toronto Ontario · CA FEI 3012147801