Identity
- Trade Name
- Lumina NRG FDA UDI
- Generic Name
- Red-light phototherapy unit, home-use FDA UDI
- Device Name
- Mini Glow PRO FDA UDI
- Model / Reference
- 6572 FDA UDI
- Description
- Mini Glow PRO FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850018806572 FDA UDI
- 510(k) Number
- K202055 FDA UDI
- FDA Product Code
- OLP FDA UDI
- GMDN Term
- Red-light phototherapy unit, home-use 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Red-light phototherapy unit, home-use
Lumina NRG by Heat In A Click Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Red-light phototherapy unit, home-use.
- Numiere — HEAT IN A CLICK LLC · Class II
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
- Heat In A Click Llc
Sources (1)
- FDA UDI 392f46c2-d5a8-44e0-acc7-7c0d1d4af00f 34 fields · synced May 30, 2026