FDA UDI
In Commercial Distribution
🇺🇸 United States
EVRL-OTC
DI: 00858985006360
·
Model: EVRL3-OTC
·
ERCHONIA CORPORATION, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- EVRL-OTC
- Primary DI
- 00858985006360
- Version / Model
- EVRL3-OTC
- Company Name
- ERCHONIA CORPORATION, LLC
- Labeler DUNS
- 004053174
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2026-02-09
- Public Version
- 1
- Public Version Date
- 2026-02-17
- Public Version Status
- New
- Public Device Record Key
- c37a6550-47c9-4cfd-b2e9-eb652ab1e7a9
Device Description
MEDICAL - Handheld Low Level Laser - OTC - 2 diodes 640nm & 405 nm 7.5 mW - includes induction charger - IFU Reduction Acne
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
- Yes
- Has Lot/Batch Number
- No
- Has Manufacturing Date
- Yes
- 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 |
|---|---|---|---|---|
| 62116 | Red/blue light phototherapy unit | A portable electrically-powered device intended to emit both red and blue light for the treatment of a facial skin condition (e.g., acne, hyperpigmentation) by the patient in the home. It includes integral lights with a controller/controlling interface (to pair with an off-the-shelf computer/smartphone), and may be available in a variety of forms (e.g., a face-worn light mask with controller, hand-held light unit). It is not intended for use with a photosensitizing agent. This is a single-patient, reusable device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00858985006360 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K251843 | 000 |