Identity
- Trade Name
- CurrentBody Skin™ FDA UDI
- Generic Name
- Cosmetic red-light phototherapy system, home-use FDA UDI
- Device Name
- The LED Eye Perfector (Model: EY-36A) is an Over-the-Counter (OTC) device intended for use in treating wrinkles within the periorbital region FDA UDI
- Model / Reference
- EY-36A FDA UDI
- Description
- The LED Eye Perfector (Model: EY-36A) is an Over-the-Counter (OTC) device intended for use in treating wrinkles within the periorbital region FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00655729008266 FDA UDI
- FDA Product Code
- OHS FDA UDI
- GMDN Term
- Cosmetic red-light phototherapy system, 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Cosmetic red-light phototherapy system, home-use
CurrentBody Skin™ by Shenzhen Kaiyan Medical Equipment Co, . Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cosmetic red-light phototherapy system, home-use.
- Silk'n — Home Skinovations , Ltd. · Class II
- BOOST LED BODY PATCH — iSMART Developments, Ltd. · Class II
- JMOON — Shenzhen Ulike Smart Electronics Co., Ltd. · Class II
- Omnilux Contour NECK & DECOLLETE — iSMART Developments, Ltd. · Class II
- Gillette Venus Silk Expert 3 — PROCTER & GAMBLE MANUFACTURING COMPANY, THE · Class II
- Dp Dermaceuticals L.E.D. FACE — iSMART Developments, Ltd. · Class II
- Iluminage — Tanda Beauty Canada, Inc · Class II
- NuFACE — Nuface · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Shenzhen Kaiyan Medical Equipment Co, . Ltd
Sources (1)
- FDA UDI a7c991a2-9f68-4e7e-b4ae-c15f3434fa83 33 fields · synced May 29, 2026