Identity
- Trade Name
- Color Case FDA UDI
- Generic Name
- Contact lens case FDA UDI
- Device Name
- Contact Lens Case, 3 Pack FDA UDI
- Model / Reference
- CC40 FDA UDI
- Description
- Contact Lens Case, 3 Pack FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00897522001482 FDA UDI
- 510(k) Number
- K130753 FDA UDI
- FDA Product Code
- LRX FDA UDI
- GMDN Term
- Contact lens case FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.5928 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Contact lens case
Color Case by Watchdog Group, LC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Contact lens case.
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- Optisource — PHOENIX HEALTHCARE SOLUTIONS, LLC · Class II
- Optisource — PHOENIX HEALTHCARE SOLUTIONS, LLC · Class II
Cleared under the same submission
K130753 also covers:
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
- Watchdog Group, LC
Sources (1)
- FDA UDI 40bd14bc-23c7-4c3b-9975-0974a7ff0df9 35 fields · synced Jun 8, 2026