Identity
- Trade Name
- HOLLYWOOD PLATINUM FDA UDI
- Generic Name
- Soft corrective contact lens, daily-wear FDA UDI
- Device Name
- Color lens(P: 0.00), 2 pcs FDA UDI
- Model / Reference
- FL-D35 Satin Gray FDA UDI
- Description
- Color lens(P: 0.00), 2 pcs FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800071352709 FDA UDI
- 510(k) Number
- K110835 FDA UDI
- FDA Product Code
- LPL FDA UDI
- GMDN Term
- Soft corrective contact lens, daily-wear FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.5925 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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: Soft corrective contact lens, daily-wear
Hollywood Platinum by GEO Medical Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- GEO Medical Co., Ltd.
Sources (1)
- FDA UDI af7a7298-cd6f-4c90-8769-7cad8efdb222 35 fields · synced May 30, 2026