510(k) Report

510(k) · Cleared

Cleared

Total30, Total30 for Astigmatism, Total30 Multifocal, Total30 Multifocal Toric, Total30 Asphere

K210436510(k) TraditionalCleared Apr 12, 202159-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

Alcon Laboratories, Inc. · LPL Lenses, Soft Contact, Daily Wear

Cleared on Apr 12, 2021 as substantially equivalent to K052560 (CooperVision, Inc., 2005) after a 59-day review. Its family tree reaches back 5 generations to 1981. 4 later devices descend from it.

Decided
Apr 12, 2021
Review
59 days
Class
Class II
Product code
LPL
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to P810005 (1981). 7 ancestors in all. 4 later devices descend from it, 2 citing it directly.

  1. Root · 5 generations backP810005 Weicon (R) (Tefilicon) Hydrophilic Contact LensCiba Vision Care · 1981
  2. 4 generations backK970746 SEE3 (Lotrafilcon a) Soft Contact LensCiba Vision Corporation · 1997
  3. 3 generations backK020139 Focus Excelens (Lotrafilcon B) Spherical, Toric and Multifocal DesignCiba Vision Corporation · 2002
  4. 2 generations backK033919 Ciba Vision (Lotrafilcon B) Spherical, Toric, Multifocal and Toric…Ciba Vision Corporation · 2004 · Recalled
  5. 1 generation backK052560 Biofinity (Comfilcon a) Soft Contact LensCooperVision, Inc. · 2005 · Recalled
  6. This deviceK210436 Total30, Total30 for Astigmatism, Total30 Multifocal, Total30…Alcon Laboratories, Inc. · 2021
  7. Descendant · cites it directly · 2 of its ownK233856 Precision1; Precision1 for Astigmatism; TOTAL30; TOTAL30 for…Alcon Laboratories, Inc. · 2023 · Recalled
  8. Descendant · 2 generations on · 1 of its ownK243909 Precision1; Precision1 for Astigmatism; Dailies Total1; Dailies…Alcon Laboratories, Inc. · 2025
  9. Descendant · 3 generations on · 0 of its ownK254052 DAILIES TOTAL1®; DAILIES TOTAL1® MultifocalAlcon Laboratories, Inc. · 2026
  10. Descendant · cites it directly · 0 of its ownK240519 Innova Vision (inifilcon A) Silicone Hydrogel (Hydrophilic) Daily…Innova Vision, Inc. · 2024

Most influential descendants

Showing 4 of 4 · See all
  • K233856Precision1; Precision1 for Astigmatism; TOTAL30; TOTAL30 for Astigmatism; TOTAL30…Alcon Laboratories, Inc. · 2023 · cites it directly2descendants
  • K243909Precision1; Precision1 for Astigmatism; Dailies Total1; Dailies Total1 for Astigmatism…Alcon Laboratories, Inc. · 2025 · 2 generations on1descendant
  • K254052DAILIES TOTAL1®; DAILIES TOTAL1® MultifocalAlcon Laboratories, Inc. · 2026 · 3 generations on0descendants
  • K240519Innova Vision (inifilcon A) Silicone Hydrogel (Hydrophilic) Daily Wear Soft Contact LensInnova Vision, Inc. · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5P810005Weicon (R) (Tefilicon) Hydrophilic Contact LensCiba Vision Care1981—
−4K970746SEE3 (Lotrafilcon a) Soft Contact LensCiba Vision Corporation1997—
−3K020139Focus Excelens (Lotrafilcon B) Spherical, Toric and Multifocal DesignCiba Vision Corporation2002—
−2K033919Ciba Vision (Lotrafilcon B) Spherical, Toric, Multifocal and Toric Multifocal…Ciba Vision Corporation20041
−1K052560Biofinity (Comfilcon a) Soft Contact LensCooperVision, Inc.20051
0 (this device)K210436Total30, Total30 for Astigmatism, Total30 Multifocal, Total30 Multifocal…Alcon Laboratories, Inc.2021—
+1K233856Precision1; Precision1 for Astigmatism; TOTAL30; TOTAL30 for Astigmatism…Alcon Laboratories, Inc.20231
+2K243909Precision1; Precision1 for Astigmatism; Dailies Total1; Dailies Total1 for…Alcon Laboratories, Inc.2025—
+3K254052DAILIES TOTAL1®; DAILIES TOTAL1® MultifocalAlcon Laboratories, Inc.2026—
+1K240519Innova Vision (inifilcon A) Silicone Hydrogel (Hydrophilic) Daily Wear Soft…Innova Vision, Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198410
200110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
202410
202510
202610
FIG. 1 — Lineage of K210436, 1981–2026Source: 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? (1)

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
*K052560Biofinity (Comfilcon a) Soft Contact Lens
Summary page 5
…mer or oligomer at pH 6 to pH 8 The predicate device has US FDA Premarket Notification 510(k) clearance for daily wear (K052560, December 6, 2005). IV. Device Description The subject device, TOTAL30TM (lehfilcon A) soft contact lenses, are made from a…
CooperVision, Inc.20051

Also cleared against K052560: 14 other devices →

What descends from it? (4)

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

NumberDeviceApplicantDecidedDescendants
K233856Precision1; Precision1 for Astigmatism; TOTAL30; TOTAL30 for Astigmatism; TOTAL30…Alcon Laboratories, Inc.20232
K240519Innova Vision (inifilcon A) Silicone Hydrogel (Hydrophilic) Daily Wear Soft Contact LensInnova Vision, Inc.20240

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 40 years and passes through 4 companies; a new generation was cleared every 4.9 years on median.
  • 4 of the 7 ancestors have a recall of any class.
  • Of its descendants, K233856 (Alcon Laboratories, Inc., 2023) has gone furthest, with 2 descendants of its own.
  • 14 other devices also cite its predicate K052560.

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. 2021, 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?

TOTAL30 (lehfilcon A) spherical soft contact lenses are indicated for the optical correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic persons with non-diseased eyes with up to approximately 1.50 diopters (D) of astigmatism that does not interfere with visual acuity. TOTAL30 Asphere (lehfilcon A) soft contact lenses are indicated for the optical correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic…

Read the full statement (291 words)

TOTAL30 (lehfilcon A) spherical soft contact lenses are indicated for the optical correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic persons with non-diseased eyes with up to approximately 1.50 diopters (D) of astigmatism that does not interfere with visual acuity.

TOTAL30 Asphere (lehfilcon A) soft contact lenses are indicated for the optical correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic persons with non-diseased eyes with up to approximately 1.50 diopters of astigmatism that does not interfere with visual acuity.

TOTAL30 for Astigmatism (lehfilcon A) toric soft contact lenses are indicated for the optical correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic persons with non-diseased eyes with up to 6.00 diopters (D) of astigmatism.

TOTAL30 Multifocal (lehfilcon A) soft contact lenses are indicated for the optical correction of presbyopia with or without refractive ametropia (myopia and hyperopia) in phakic or aphakic persons with non-diseased eyes who may require a reading addition of +3.00 diopters (D) or less and who may have up to approximately 1.50 diopters (D) of astigmatism that does not interfere with visual acuity.

TOTAL30 Multifocal Toric (lehfilcon A) soft contact lenses are indicated for the optical correction of presbyopia with or without refractive ametropia (myopia and hyperopia) in phakic or aphakic persons with non-diseased eyes who may require a reading addition of +3.00 diopters (D) or less and who may have up to 6.00 diopters (D) of astigmatism.

The lenses are to be prescribed for daily wear, with removal for cleaning and disinfection (chemical, not heat) prior to reinsertion, or disposal, as recommended by the eye care professional. Lenses should be discarded and replaced with a new pair each month, or more often, if recommended by the eye care professional.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K210436: Total30, Total30 for Astigmatism, Total30 Multifocal, Total30 Multifocal Toric, Total30 Asphere.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K210436

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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