Identity
- Trade Name
- Q-Rejuvalight Pro Facewear FDA UDI
- Generic Name
- Red/blue light phototherapy unit FDA UDI
- Model / Reference
- P19-0023 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08719327598719 FDA UDI
- 510(k) Number
- K230042 FDA UDI
- FDA Product Code
- OHS FDA UDIOLP FDA UDI
- GMDN Term
- Red/blue light phototherapy unit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Cosmetic red-light phototherapy system, home-useRed/blue light phototherapy unit
Q-Rejuvalight Pro Facewear by Light Tree Ventures Europe B.V. — 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
- Light Tree Ventures Europe B.V.
Sources (1)
- FDA UDI fc5fe225-7df4-4504-a6a6-a2be3e742a12 33 fields · synced May 31, 2026