Identity
- Trade Name
- Equate FDA UDI
- Generic Name
- Contact lens case FDA UDI
- Device Name
- EQ Contact Lens Case 1PK FDA UDI
- Model / Reference
- 581880437 FDA UDI
- Description
- EQ Contact Lens Case 1PK FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06971531013644 FDA UDI
- 510(k) Number
- K172925 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
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
Yes
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
Yes
FDA UDI
Liquid Chemical FDA UDI
Category: Contact lens case
Equate by Walmart Stores — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Deep Well Lens Case (Ribbed) — Paragon Vision Sciences · Class II
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- Optisource — PHOENIX HEALTHCARE SOLUTIONS, LLC · Class II
Cleared under the same submission
K172925 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
- Walmart Stores
Sources (1)
- FDA UDI 6980cbf8-35cf-4548-8787-59034ab2fc8e 35 fields · synced May 30, 2026