510(k) Report

510(k) · Cleared

Cleared

Proclear Toric XR, Proclear Multifocal XR, Proclear Multifocal Toric, Proclear Sphere & Asphere, Toric Contact Lenses

K112302510(k) TraditionalCleared Dec 21, 2011132-day reviewClass II21 CFR 886.5925

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

CooperVision, Inc. · LPL Lenses, Soft Contact, Daily Wear

Cleared on Dec 21, 2011 as substantially equivalent to K110099 (CooperVision, Inc., 2011) and 1 other predicate after a 132-day review. Its family tree reaches back 4 generations to 2001. 6 later devices descend from it.

Decided
Dec 21, 2011
Review
132 days
Class
Class II
Product code
LPL
Recalls
None
Predicates
2

Its longest line of descent runs back 4 generations to K003136 (2001). 12 ancestors in all, the oldest K952152 (1995). 6 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2008: 1 other ancestor2005: 2 other ancestors2003: 1 other ancestor1998: 1 other ancestor1997: 1 other ancestor1995: 1 other ancestor2000: 1 other ancestor2017: 1 descendant cleared2013: 1 descendant cleared2018: 1 descendant cleared2020: 1 descendant cleared2022: 1 descendant cleared2026: 1 descendant clearedK003136 · Ocular Sciences, Inc. Biomedics 52 (Ocufilcon D) UV Blocking Daily Wear Soft Contact Lens · Ocular Sciences Puerto Rico, Inc. · 2001K020389 · Biomedics 52 (Ocufilcon B) UV Blocking Daily Wear Soft Contact Lens · Ocular Sciences · 2002K061948 · Proclear (Omafilcon a) Daily Disposable/Daily Wear Soft Contact Lens · CooperVision, Inc. · 2006 · recalledK110099 · Proclear Toric XR Soft (Hydrophilic) Contact Lens; Proclear Multifocal XR Soft (Hydrophilic) Contact Lens; Proclear Mult · CooperVision, Inc. · 20111995200020052010201520202025
  1. Root · 4 generations backK003136 Ocular Sciences, Inc. Biomedics 52 (Ocufilcon D) UV Blocking Daily…Ocular Sciences Puerto Rico, Inc. · 2001
  2. 3 generations backK020389 Biomedics 52 (Ocufilcon B) UV Blocking Daily Wear Soft Contact LensOcular Sciences · 2002
  3. 2 generations backK061948 Proclear (Omafilcon a) Daily Disposable/Daily Wear Soft Contact LensCooperVision, Inc. · 2006 · Recalled
  4. 1 generation backK110099 Proclear Toric XR Soft (Hydrophilic) Contact Lens; Proclear…CooperVision, Inc. · 2011
  5. This deviceK112302 Proclear Toric XR, Proclear Multifocal XR, Proclear Multifocal…CooperVision, Inc. · 2011
  6. Descendant · cites it directly · 4 of its ownK162223 Aveo 1-DAY Aspheric Soft Contact Lens (omafilcon A)Supervision Optimax Sdn Bhd · 2017
  7. Descendant · cites it directly · 1 of its ownK180985 Aveo (omafilcon A) Soft (Hydrophilic) Contact LensesSupervision Optimax Sdn Bhd · 2018
  8. Descendant · 2 generations on · 0 of its ownK253885 PUSCON WATER BALANCE-1DAY TINT (omafilcon A) SOFT (HYDROPHILIC)…Geo Medical CO., LTD. · 2026
  9. Descendant · 2 generations on · 0 of its ownK213983 Eye Secret 59 UV Aspheric (Omafilcon A) Soft (Hydrophilic) Contact…Yung Sheng Optical Co., Ltd. · 2022
  10. Descendant · cites it directly · 0 of its ownK201013 Optixon 1-DayOptixon, Inc. · 2020

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2013: 12017: 12018: 12020: 12022: 12026: 1
2013high 1 (2013) · low 0 (2014)2026

Most influential descendants

Showing 5 of 6 · See all
  • K162223Aveo 1-DAY Aspheric Soft Contact Lens (omafilcon A)Supervision Optimax Sdn Bhd · 2017 · cites it directly4descendants
  • K180985Aveo (omafilcon A) Soft (Hydrophilic) Contact LensesSupervision Optimax Sdn Bhd · 2018 · cites it directly1descendant
  • K253885PUSCON WATER BALANCE-1DAY TINT (omafilcon A) SOFT (HYDROPHILIC) CONTACT LENS; PUSCON…Geo Medical CO., LTD. · 2026 · 2 generations on0descendants
  • K213983Eye Secret 59 UV Aspheric (Omafilcon A) Soft (Hydrophilic) Contact Lens for Daily WearYung Sheng Optical Co., Ltd. · 2022 · 2 generations on0descendants
  • K201013Optixon 1-DayOptixon, Inc. · 2020 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K003136Ocular Sciences, Inc. Biomedics 52 (Ocufilcon D) UV Blocking Daily Wear Soft…Ocular Sciences Puerto Rico, Inc.2001—
−3K020389Biomedics 52 (Ocufilcon B) UV Blocking Daily Wear Soft Contact LensOcular Sciences2002—
−2K061948Proclear (Omafilcon a) Daily Disposable/Daily Wear Soft Contact LensCooperVision, Inc.20061
−1K110099Proclear Toric XR Soft (Hydrophilic) Contact Lens; Proclear Multifocal XR Soft…CooperVision, Inc.2011—
0 (this device)K112302Proclear Toric XR, Proclear Multifocal XR, Proclear Multifocal Toric, Proclear…CooperVision, Inc.2011—
+1K162223Aveo 1-DAY Aspheric Soft Contact Lens (omafilcon A)Supervision Optimax Sdn Bhd2017—
+1K180985Aveo (omafilcon A) Soft (Hydrophilic) Contact LensesSupervision Optimax Sdn Bhd2018—
+2K253885PUSCON WATER BALANCE-1DAY TINT (omafilcon A) SOFT (HYDROPHILIC) CONTACT LENS…Geo Medical CO., LTD.2026—
+2K213983Eye Secret 59 UV Aspheric (Omafilcon A) Soft (Hydrophilic) Contact Lens for…Yung Sheng Optical Co., Ltd.2022—
+1K201013Optixon 1-DayOptixon, Inc.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
199710
199810
200010
200310
200520
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201310
201710
201810
202010
202210
202610
FIG. 1 — Lineage of K112302, 2001–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in LPL? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new LPL device

  1. #1 K243868 Pegavision (Toufilcon B) Daily Disposable Soft…score 16.8 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K110099Proclear Toric XR Soft (Hydrophilic) Contact Lens; Proclear Multifocal XR Soft…
Summary page 3
…ns is to be discarded after each removal 7. Predicate Device(s) Proclear Multifocal, Toric and Multifocal Toric (Omafilcon A) Soft Contact Lenses (K110099) Proclear Sphere, Asphere, Toric, Multifocal and Multifocal Toric (Omnafllcon A) Soft Contact Lenses (K061948)…
CooperVision, Inc.2011—
*K061948Proclear (Omafilcon a) Daily Disposable/Daily Wear Soft Contact Lens
Summary page 3
…(Omafilcon A) Soft Contact Lenses (K110099) Proclear Sphere, Asphere, Toric, Multifocal and Multifocal Toric (Omnafllcon A) Soft Contact Lenses (K061948) 8. Characteristics of Substantial Equivalence The soft contact lenses have the following similarities to the pred…
CooperVision, Inc.20061

Also cleared against K110099: 1 other device →

What descends from it? (6)

4 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K162223Aveo 1-DAY Aspheric Soft Contact Lens (omafilcon A)Supervision Optimax Sdn Bhd20174
K180985Aveo (omafilcon A) Soft (Hydrophilic) Contact LensesSupervision Optimax Sdn Bhd20181
K201013Optixon 1-DayOptixon, Inc.20200
K123202Proclear (Omafilcon a) Soft Hydrophilic) Contact LensCooperVision, Inc.20130

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 10 years and passes through 3 companies; a new generation was cleared every 4.5 years on median.
  • 1 of the 12 ancestors has a recall of any class.
  • Of its descendants, K162223 (Supervision Optimax Sdn Bhd, 2017) has gone furthest, with 4 descendants of its own.
  • 1 other device also cites its predicate K110099.

How does its category compare?

All LPL devices

LPL Lenses, Soft Contact, Daily Wear: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · LPL

12in 2025

2007: 32008: 102009: 62010: 92011: 122012: 122013: 172014: 152015: 122016: 212017: 92018: 212019: 112020: 102021: 82022: 92023: 102024: 122025: 122026 (partial year): 10
2007high 21 (2016) · low 3 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LPL

202in 2025

2007: 281 days median2008: 104 days median2009: 260 days median2010: 244 days median2011: 170 days median2012: 131 days median2013: 135 days median2014: 102 days median2015: 120 days median2016: 112 days median2017: 98 days median2018: 56 days median2019: 115 days median2020: 158 days median2021: 88 days median2022: 212 days median2023: 167 days median2024: 128 days median2025: 202 days median2026 (partial year): 90 days median
2007high 281 (2007) · low 56 (2018)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · LPL

1in 2025

2007: 12009: 12011: 52012: 12014: 12015: 12017: 112020: 12022: 12025: 12026 (partial year): 1
2007high 11 (2017) · low 0 (2008)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LPL

216in 2025

2007: 2802008: 2142009: 1372010: 2222011: 3772012: 2502013: 1512014: 1792015: 1612016: 1932017: 2802018: 2572019: 2052020: 1172021: 1102022: 1262023: 1782024: 2972025: 216
2007high 377 (2011) · low 110 (2021)2025

MAUDE reports naming product code LPL, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
200732811280
2008101040214
200962601137
201092440222
2011121705377
2012121311250
2013171350151
2014151021179
2015121201161
2016211120193
201799811280
201821560257
2019111150205
2020101581117
20218880110
202292121126
2023101670178
2024121280297
2025122021216
202610901—

What is it indicated for?

Proclear Multifotcal Toric (omafilcon A) Soft (Hydrophilic) Contact Lenses are indicated for daily wear for the correction of visual acuity in aphakic and not-aphakic persons with nondiseased eyes that are myopic or hyperopic which, possess astigmatism to -5.75 diopters or less, and are presbyopic. Proclear Multifocal XR (omnafilcon A) Soft (Hydrophilic) Contact Lenses are indicated for daily wear for the correction of visual acuity in aphakic and…

Read the full statement (414 words)

Proclear Multifotcal Toric (omafilcon A) Soft (Hydrophilic) Contact Lenses are indicated for daily wear for the correction of visual acuity in aphakic and not-aphakic persons with nondiseased eyes that are myopic or hyperopic which, possess astigmatism to -5.75 diopters or less, and are presbyopic.

Proclear Multifocal XR (omnafilcon A) Soft (Hydrophilic) Contact Lenses are indicated for daily wear for the correction of visual acuity in aphakic and not-aphakic persons with nondiseased eyes that are myopic or hyperopic and are presbyopic. The lenses may be worn by persons who exhibit astigmatism of 0.75 diopters or less that does not interfere with visual acuity.

Proclear Tonec XR (omafilcon A) Soft (Hydrophilic) Contact Lenses are indicated for daily wear for the correction of visual acuity in aphakic and not-aphakic persons with non-diseased eyes that are myopic or hyperopic which possess astigmatism corrections to -5.75 diopters.

Proclear Sphere and Asphere: (omafilcon A) Soft (hydrophilic) Contact Lenses are indicated for daily wear for the correction of visual acuity in non-aphakic persons with non-diseased eyes that are myopic or hyperopic and exhibit astigmatism of 2.0013 or less that does not interfere with visual acuity.

Proclear Torie: (omafilcon A) Soft (hydrophilic) Contact Lenses are indicated for daily wear for the correction of visual acuity in non-aphakic persons with non-diseased eyes that are myopic or hyperopic The lens may be worn by persons who have astigmatism of 5.000 or less.

Proclear Multifocal: (omafilcon A) Soft (hydrophilic) Contact Lenses are indicated for daily wear for the correction of refractive arnetropia (myopia, hyperopia, and astigmatism) and presbyopia in non-aphakic persons with non-diseased eyes. The lens may be worn by persons who have astigmatism of 2.000 or less that does not interfere with visual acuity.

Proclear (oinafilcon A) Soft (hydrophilic) Contact Lenses may provide improved comfort for contact lens wearers who experience mild discomfort or symptoms related to dryness during lens wear associated with Evaporative Tear Deficiency or from Aqueous Tear Deficiency (non-Sjogren's only).

Daily wear replacement schedules may vary from patient to patient and should be decided by eyecare practitioners in consultation with their patients-

FREQUENT PLANNED REPLACEMENT WEAR

When prescribed for frequent planned replacement wear the lenses are to be cleaned, rinsed and disinfected each time they are removed, from the patients' eye and discarded after the recommended wearing period prescribed by the eye care practitioner. The lenses may be disinfected using a chemical disinfection system

DISPOSABLE WEAR

When prescribed for Daily Disposable Wear the lens is to be discarded after each removal

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K112302: Proclear Toric XR, Proclear Multifocal XR, Proclear Multifocal Toric, Proclear Sphere & Asphere, Toric Contact Lenses.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K112302

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026