Identity
- Trade Name
- CurrentBody™ FDA UDI
- Generic Name
- Cosmetic red-light phototherapy system, home-use FDA UDI
- Device Name
- The CurrentBody™ LED 4 in 1 Zone Facial Mapping Mask (Models: Mk-90C) is an over the counter device, specifically indicated to treat mild to moderate acne vulgaris of the face and use in the treatment of full-face wrinkles FDA UDI
- Model / Reference
- MK-90C FDA UDI
- Description
- The CurrentBody™ LED 4 in 1 Zone Facial Mapping Mask (Models: Mk-90C) is an over the counter device, specifically indicated to treat mild to moderate acne vulgaris of the face and use in the treatment of full-face wrinkles FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00731093153914 FDA UDI
- FDA Product Code
- OHS FDA UDIOLP 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™ 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 7c2f6f93-57df-48db-b1dc-06ba3e00e251 33 fields · synced May 31, 2026