Vista Plus

FDA UDI

Class II (US FDA UDI)

by Optimax Eyewear Inc

Identity

Trade Name: Vista Plus FDA UDI
Generic Name: Soft corrective contact lens, daily-disposable FDA UDI
Device Name: Vista Plus 10PK-11 FDA UDI
Model / Reference: 181-0000035N1100000000 FDA UDI
Description: Vista Plus 10PK-11 FDA UDI

Identifiers

Primary DI / UDI-DI: 07290117300534 FDA UDI
FDA Product Code: LPL FDA UDI
MVN 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

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-disposable

Vista Plus by Optimax Eyewear Inc — 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: Optimax Eyewear Inc

Sources (1)

FDA UDI 704f1cf1-9893-41bd-b4cb-d8b5fb61387f 33 fields · synced May 30, 2026