Identity
- Trade Name
- ZonedIn Contact Lenses FDA UDI
- Generic Name
- Soft corrective contact lens, daily-disposable FDA UDI
- Device Name
- Daily disposable etafilcon A contact lens -0.50 power FDA UDI
- Model / Reference
- 710050 FDA UDI
- Description
- Daily disposable etafilcon A contact lens -0.50 power FDA UDI
Identifiers
- Catalog Number
- 710050 FDA UDI
- Primary DI / UDI-DI
- 00810040140006 FDA UDI
- FDA Product Code
- LPL FDA UDIMVN FDA UDI
- GMDN Term
- Soft corrective contact lens, daily-disposable 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
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Category: Soft corrective contact lens, daily-disposable
ZonedIn Contact Lenses by Zonedin Vision Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Zonedin Vision Llc
Sources (1)
- FDA UDI 275a995b-1260-4e96-859d-6a1d2b9bcf88 34 fields · synced Jun 1, 2026