Identity
- Trade Name
- JOVS IPL Hair Removal Device FDA UDI
- Generic Name
- Intense pulsed light skin surface treatment system FDA UDI
- Model / Reference
- JR8 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06973698659758 FDA UDI
- 510(k) Number
- K231800 FDA UDI
- FDA Product Code
- OHT FDA UDI
- GMDN Term
- Intense pulsed light skin surface treatment system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
JOVS IPL Hair Removal Device by Shenzhen Qianyu Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Shenzhen Qianyu Technology Co., Ltd.
Sources (1)
- FDA UDI 28084aee-3e6b-473f-b53e-489c03707353 34 fields · synced Jun 6, 2026