clearall-day Toric

FDA UDI

Class II (US FDA UDI)

by Clearlab Sg Pte. Ltd.

Identity

Trade Name: clearall-day Toric FDA UDI
Generic Name: Soft corrective contact lens, daily-wear FDA UDI
Device Name: The clearall-day Toric (hioxifilcon A) Soft Contact Lenses for daily wear are indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with myopia or hyperopia and may have astigmatism of 7.00D of astigmatism or less. Eyecare practitioners may prescribe the lenses for frequent/planned replacement wear, with cleaning, disinfection and scheduled replacement. When prescribed for frequent/planned replacement wear, the lens may be cleaned and disinfected using a chemical (not heat) lens care system. FDA UDI
Model / Reference: clearall-day Toric FDA UDI
Description: The clearall-day Toric (hioxifilcon A) Soft Contact Lenses for daily wear are indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with myopia or hyperopia and may have astigmatism of 7.00D of astigmatism or less. Eyecare practitioners may prescribe the lenses for frequent/planned replacement wear, with cleaning, disinfection and scheduled replacement. When prescribed for frequent/planned replacement wear, the lens may be cleaned and disinfected using a chemical (not heat) lens care system. FDA UDI

Identifiers

Primary DI / UDI-DI: 08887861972682 FDA UDI
510(k) Number: K052290 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

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

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Soft corrective contact lens, daily-wear

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

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

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HAPA KRISTIN — INTEROJO INC. · Class II
Loox — Camden Passage Inc · Class II
ArtMost SoftOK Daily Wear Soft Contact Lens — SEINOH OPTICAL CO., LTD. · Class II
ArtMost SoftOK Daily Wear Soft Contact Lens — SEINOH OPTICAL CO., LTD. · Class II

Cleared under the same submission

K052290 also covers:

clearall-day — CLEARLAB SG PTE. LTD.

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: Clearlab Sg Pte. Ltd.

Sources (1)

FDA UDI a75f2408-f3e6-463f-b625-1c9c940b7a61 35 fields · synced Jun 6, 2026