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Sign in to claim this brandPHYSIOHAB LLC
US
Last updated May 25, 2026
What PHYSIOHAB LLC makes
PhysioHab LLC manufactures blue, red, and infrared phototherapy lamps designed for therapeutic light treatment applications. These devices are primarily used in medical settings to deliver targeted light wavelengths for conditions such as wound healing, pain management, and skin rejuvenation.
The company’s phototherapy lamps fall under FDA Class II devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The products are regulated under U.S. medical device laws and comply with applicable FDA requirements for Class II devices.
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 PhysioHab LLC manufacture?
PhysioHab LLC specializes in phototherapy lamps that emit blue, red, and infrared light. These devices are designed for therapeutic applications, such as wound healing, pain management, and skin rejuvenation, and are primarily intended for use in medical settings.
Where is PhysioHab LLC based?
PhysioHab LLC is based in the United States. The company’s devices are developed and manufactured under U.S. regulatory standards.
Which regulatory registries list PhysioHab LLC’s devices?
PhysioHab LLC’s phototherapy lamps are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S. under applicable regulations.
How are PhysioHab LLC’s devices classified by regulatory authorities?
PhysioHab LLC’s phototherapy lamps fall under FDA Class II classification. This classification is assigned based on the level of risk associated with the device, with Class II devices requiring special controls in addition to 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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- 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
- 122389660
Catalogue (9)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Onlux | OLF3009 | FDA UDI | Class II | Active |
| Onlux | OLS3005 | FDA UDI | Class II | Active |
| Onlux | OLE3006 | FDA UDI | Class II | Active |
| Onlux | OLA3001 | FDA UDI | Class II | Active |
| Onlux | OLN3004 | FDA UDI | Class II | Active |
| Onlux | OLH3007 | FDA UDI | Class II | Active |
| Onlux | OLKA3003 | FDA UDI | Class II | Active |
| Onlux | OLK3002 | FDA UDI | Class II | Active |
| Onlux | OLL3003 | FDA UDI | Class II | Active |
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