Identity
- Trade Name
- Diode Laser Hair Removal FDA UDI
- Generic Name
- Home-use laser epilator FDA UDI
- Model / Reference
- LHR-V8S-810 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06940481500085 FDA UDI
- 510(k) Number
- K230090 FDA UDI
- FDA Product Code
- OHT FDA UDI
- GMDN Term
- Home-use laser epilator 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
No
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Home-use laser epilator
Diode Laser Hair Removal by Wuhan Lotuxs Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Home-use laser epilator.
- Diode Laser Hair Removal — Wuhan Lotuxs Technology Co., Ltd. · Class II
- Diode Laser Hair Removal — Wuhan Lotuxs Technology Co., Ltd. · Class II
- Diode Laser Hair Removal — Wuhan Lotuxs Technology Co., Ltd. · Class II
- Diode Laser Hair Removal — Wuhan Lotuxs Technology Co., Ltd. · Class II
- Diode Laser Hair Removal — Wuhan Lotuxs Technology Co., Ltd. · Class II
Cleared under the same submission
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
- Wuhan Lotuxs Technology Co., Ltd.
Sources (1)
- FDA UDI f06af7cf-4f99-4320-bc20-6a13b8112a23 33 fields · synced May 30, 2026