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clear1-day Multifocal

FDA UDI

Class II (US FDA UDI)

by Clearlab Sg Pte. Ltd.

Identity

Trade Name
clear1-day Multifocal FDA UDI
Generic Name
Soft corrective contact lens, daily-wear FDA UDI
Device Name
The clear1-day Multifocal (hioxifilcon A) Daily Disposable Soft Contact Lens is available as a single vision multifocal lens. The hydrophilic nature of this material allows the lens to become soft and pliable when immersed in an aqueous solution. The non-ionic lens material, (hioxifilcon A) is a ultra high molecular weight random copolymer of 2-hydroxyethyl methacrylate (2-HEMA) and 2,3-Dihydroxpropyl Methacrylate (Glycerol Methacrylate, GMA) cross-linked with ethylene glycol dimethacrylate. It consists of 42% hioxifilcon A and 58% water by weight when immersed in a buffered saline solution. The lens is available with a pale blue visibility- handling tint, color additive 'Reactive Blue # 4', 21 CFR part 73.3121. The United States Adopted Names Council (USAN) has adopted the (hioxifilcon A) name. In the hydrated state, the lens conforms to the curvature of the eye covering the cornea and extending slightly beyond the limbus forming a colorless, transparent optical surface. The hydrophilic properties of the lens require that it be maintained in a fully hydrated state in a solution compatible with the eye. If the lens dries out, it will become hard and appear somewhat warped however, it ill return to its proper configuration when completely rehydrated in the proper storage solution. FDA UDI
Model / Reference
clear1-day Multifocal FDA UDI
Description
The clear1-day Multifocal (hioxifilcon A) Daily Disposable Soft Contact Lens is available as a single vision multifocal lens. The hydrophilic nature of this material allows the lens to become soft and pliable when immersed in an aqueous solution. The non-ionic lens material, (hioxifilcon A) is a ultra high molecular weight random copolymer of 2-hydroxyethyl methacrylate (2-HEMA) and 2,3-Dihydroxpropyl Methacrylate (Glycerol Methacrylate, GMA) cross-linked with ethylene glycol dimethacrylate. It consists of 42% hioxifilcon A and 58% water by weight when immersed in a buffered saline solution. The lens is available with a pale blue visibility- handling tint, color additive 'Reactive Blue # 4', 21 CFR part 73.3121. The United States Adopted Names Council (USAN) has adopted the (hioxifilcon A) name. In the hydrated state, the lens conforms to the curvature of the eye covering the cornea and extending slightly beyond the limbus forming a colorless, transparent optical surface. The hydrophilic properties of the lens require that it be maintained in a fully hydrated state in a solution compatible with the eye. If the lens dries out, it will become hard and appear somewhat warped however, it ill return to its proper configuration when completely rehydrated in the proper storage solution. FDA UDI

Identifiers

Primary DI / UDI-DI
08887861972620 FDA UDI
510(k) Number
K080632 FDA UDI
FDA Product Code
LPL FDA UDI
GMDN Term
Soft corrective contact lens, daily-wear 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Soft corrective contact lens, daily-wear

clear1-day Multifocal by Clearlab Sg Pte. Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Soft corrective contact lens, daily-wear.

Cleared under the same submission

K080632 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Clearlab Sg Pte. Ltd.

Sources (1)

  • FDA UDI 66349ced-6c46-440c-88b4-36c238ed31b4 35 fields · synced Jun 1, 2026