FDA Device Intelligence
HomeCLEARLAB SG PTE. LTD. › clearall-day Toric

clearall-day Toric

CLEARLAB SG PTE. LTD. · Model clearall-day Toric · UDI-DI 08887861972682

LPL Prescription
1
510(k) clearances
4,868
Adverse events
70
Recalls
133
Facilities

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.

Recalls

DateFirmReason
2025-09-30Alcon Research LLCPotential for a weak seal in some units resulting in compromise in sterility.
2025-06-12Johnson & Johnson Vision Care, Inc.Due to defects (bubbles/voids) identified during standard finished goods testing
2024-08-08Alcon Research LLCMaterial with a quality issue was used in contact lens production, so contact lenses may not meet quality and/or performance standards for the entirety of their labeled shelf life,
2023-02-14CooperVision, Inc.The lenses manufactured in the affected lot were made with a misaligned axis resulting in lenses with the incorrect power.
2022-12-27CooperVision, Inc.Lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity.
2021-05-19CooperVision Inc.Misaligned placement of an axis mark can cause the patient to experience blurred vision
2021-05-19CooperVision Inc.Misaligned placement of an axis mark can cause the patient to experience blurred vision
2021-05-19CooperVision Inc.Misaligned placement of an axis mark can cause the patient to experience blurred vision
2021-05-19CooperVision Inc.Misaligned placement of an axis mark can cause the patient to experience blurred vision
2021-05-19CooperVision Inc.Misaligned placement of an axis mark can cause the patient to experience blurred vision

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.