Identity
- Trade Name
- Nerve Reviver FDA UDI
- Generic Name
- Blue/red/infrared phototherapy lamp FDA UDI
- Device Name
- The Nerve Reviver Neuroglow Wrap delivers soothing infrared light therapy through a flexible, comfortable design that contours to the body. Using therapeutic infrared LED technology, it helps relax muscles, ease minor aches and stiffness, and support healthy circulation. Portable, reusable, and easy to clean, Neuroglow provides safe, non-invasive relief that can be used at home, in clinics, or on the go. FDA UDI
- Model / Reference
- Neuroglow FDA UDI
- Description
- The Nerve Reviver Neuroglow Wrap delivers soothing infrared light therapy through a flexible, comfortable design that contours to the body. Using therapeutic infrared LED technology, it helps relax muscles, ease minor aches and stiffness, and support healthy circulation. Portable, reusable, and easy to clean, Neuroglow provides safe, non-invasive relief that can be used at home, in clinics, or on the go. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860011592839 FDA UDI
- FDA Product Code
- ILY FDA UDI
- GMDN Term
- Blue/red/infrared phototherapy lamp FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Blue/red/infrared phototherapy lamp
Nerve Reviver by Protocol Solutions Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Protocol Solutions Llc
Sources (1)
- FDA UDI de2cbca9-21d6-4e19-92a5-a25defece9c4 34 fields · synced May 31, 2026