FDA UDI
In Commercial Distribution
🇺🇸 United States
Lumina NRG
DI: 00850018806572
·
Model: 6572
·
Heatinaclick LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Lumina NRG
- Primary DI
- 00850018806572
- Version / Model
- 6572
- Company Name
- Heatinaclick LLC
- Labeler DUNS
- 043038693
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2025-01-31
- Public Version
- 1
- Public Version Date
- 2025-02-10
- Public Version Status
- New
- Public Device Record Key
- 392f46c2-d5a8-44e0-acc7-7c0d1d4af00f
Device Description
Mini Glow PRO
Device Characteristics
- Single Use
- No
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- Yes
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| OLP | Over-The-Counter Powered Light Based Laser For Acne | General, Plastic Surgery | 878.4810 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 66591 | Red-light phototherapy unit, home-use | An electrically-powered, patient-worn device designed be used by a layperson in the home (may additionally be used by a healthcare professional in a clinical setting) to emit red light for phototherapy primarily to treat musculoskeletal symptoms (e.g., arthritis pain, spasm, stiffness) and increase muscle relaxation through localized modification of cellular metabolism and/or improvement of blood circulation. It is in the form of a wearable thin adhesive hydrogel patch with integrated light-emitting diodes (LEDs) designed to be applied to the affected area. This is a reusable device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00850018806572 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K202055 | 000 |