Identity
- Trade Name
- Silk'n FDA UDI
- Generic Name
- Penile sexual vibrator FDA UDI
- Model / Reference
- Tightra NA FDA UDI
Identifiers
- Catalog Number
- 7290112450067 FDA UDI
- Primary DI / UDI-DI
- 17290112450064 FDA UDI
- FDA Product Code
- KXQ FDA UDI
- GMDN Term
- Penile sexual vibrator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.5960 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Penile sexual vibrator
Silk'n by Home Skinovations , 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
- Home Skinovations , Ltd.
Sources (1)
- FDA UDI 08e540a6-47f6-4fd4-94bb-a18429b8c836 35 fields · synced May 30, 2026