ZonedIn Contact Lenses

FDA UDI

Class II (US FDA UDI)

by Zonedin Vision Llc

Identity

Trade Name: ZonedIn Contact Lenses FDA UDI
Generic Name: Soft corrective contact lens, daily-disposable FDA UDI
Device Name: Hioxifilcon D monthly soft contact lens trial +2.75 power (Blisters) FDA UDI
Model / Reference: HD1275BL FDA UDI
Description: Hioxifilcon D monthly soft contact lens trial +2.75 power (Blisters) FDA UDI

Identifiers

Catalog Number: HD1275BL FDA UDI
Primary DI / UDI-DI: 00810040145834 FDA UDI
FDA Product Code: MVN FDA UDI
LPL 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

Yes

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

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 0c843829-c33e-4841-80f4-77558aac2a97 34 fields · synced May 30, 2026