510(k) Report

510(k) · Cleared

Cleared

Frequency 55 UV (Methafilcon a) Hydrophilic Contact Lens for Daily Wear (Clear and Tinted with UV Blocker)

K982997510(k) TraditionalCleared Jan 20, 1999146-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

Aspect Vision Care, Ltd. · LPL Lenses, Soft Contact, Daily Wear

Cleared on Jan 20, 1999 as substantially equivalent to K973063 (Aspect Vision Care, Ltd., 1997) after a 146-day review. Its family tree reaches back 3 generations to 1995. 6 later devices descend from it.

Decided
Jan 20, 1999
Review
146 days
Class
Class II
Product code
LPL
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K951893 (1995). 4 ancestors in all. 6 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1996: 1 other ancestor1999: 1 descendant cleared2002: 1 descendant cleared2018: 2 descendants cleared2025: 1 descendant cleared2019: 1 descendant clearedReference device: K971164 · Frequency 55 (Methafilcon a) Hydrophilic Contact Lens · Aspect Vision Care, Ltd. · 1997K951893 · Lifestyle 55 (Ocufilcon D) Hydrophilic Contact Lens Lifestyle Frequency 55 (Ocufilcon D) Ghydrophilic Contact Lens · Permeable Technologies, Inc. · 1995×2: 2 generations cleared close together, K971164 (1997), K973063 (1997) 1995200020052010201520202025
  1. Root · 3 generations backK951893 Lifestyle 55 (Ocufilcon D) Hydrophilic Contact Lens Lifestyle…Permeable Technologies, Inc. · 1995
  2. 2 generations backK971164 Frequency 55 (Methafilcon a) Hydrophilic Contact LensAspect Vision Care, Ltd. · 1997
  3. 1 generation backK973063 Frequency 55 (Methafilcon a) Hydrophilic Contact Lens for Daily WearAspect Vision Care, Ltd. · 1997 · Recalled
  4. This deviceK982997 Frequency 55 UV (Methafilcon a) Hydrophilic Contact Lens for Daily…Aspect Vision Care, Ltd. · 1999
  5. Descendant · cites it directly · 3 of its ownK020392 Frequency 55 UV (Methafilcon a) Soft (Hydrophlic) Contact Lens for…CooperVision, Inc. · 2002
  6. Descendant · 2 generations on · 2 of its ownK182247 ILICON (ocufilcon D) Soft (Hydrophilic) Daily Wear Contact Lenses…Vizionfocus, Inc. · 2018
  7. Descendant · cites it directly · 1 of its ownK993252 Methafilcon a Soft Hydrophilic Contact Lenses, Frequency 55…CooperVision, Inc. · 1999
  8. Descendant · 2 generations on · 0 of its ownK243953 Aurora (ocufilcon D) Soft (Hydrophilic) Daily Wear Contact Lens…Vizionfocus, Inc. · 2025
  9. Descendant · 3 generations on · 0 of its ownK192225 Legacy (Ocufilcon D) Performance- Tinted Soft (Hydrophilic) Daily…Vizionfocus, Inc. · 2019

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

1999: 12002: 12018: 22019: 12025: 1
1999high 2 (2018) · low 0 (2000)2026

Most influential descendants

Showing 5 of 6 · See all
  • K020392Frequency 55 UV (Methafilcon a) Soft (Hydrophlic) Contact Lens for Daily WearCooperVision, Inc. · 2002 · cites it directly3descendants
  • K182247ILICON (ocufilcon D) Soft (Hydrophilic) Daily Wear Contact Lenses (Tinted, Color)Vizionfocus, Inc. · 2018 · 2 generations on2descendants
  • K993252Methafilcon a Soft Hydrophilic Contact Lenses, Frequency 55, Frequency 55 UV (to BE…CooperVision, Inc. · 1999 · cites it directly1descendant
  • K243953Aurora (ocufilcon D) Soft (Hydrophilic) Daily Wear Contact Lens (Tinted, Color)Vizionfocus, Inc. · 2025 · 2 generations on0descendants
  • K192225Legacy (Ocufilcon D) Performance- Tinted Soft (Hydrophilic) Daily Wear Contact LensesVizionfocus, Inc. · 2019 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K951893Lifestyle 55 (Ocufilcon D) Hydrophilic Contact Lens Lifestyle Frequency 55…Permeable Technologies, Inc.1995—
−2K971164Frequency 55 (Methafilcon a) Hydrophilic Contact LensAspect Vision Care, Ltd.1997—
−1K973063Frequency 55 (Methafilcon a) Hydrophilic Contact Lens for Daily WearAspect Vision Care, Ltd.19971
0 (this device)K982997Frequency 55 UV (Methafilcon a) Hydrophilic Contact Lens for Daily Wear (Clear…Aspect Vision Care, Ltd.1999—
+1K020392Frequency 55 UV (Methafilcon a) Soft (Hydrophlic) Contact Lens for Daily WearCooperVision, Inc.2002—
+2K182247ILICON (ocufilcon D) Soft (Hydrophilic) Daily Wear Contact Lenses (Tinted…Vizionfocus, Inc.2018—
+1K993252Methafilcon a Soft Hydrophilic Contact Lenses, Frequency 55, Frequency 55 UV…CooperVision, Inc.1999—
+2K243953Aurora (ocufilcon D) Soft (Hydrophilic) Daily Wear Contact Lens (Tinted, Color)Vizionfocus, Inc.2025—
+3K192225Legacy (Ocufilcon D) Performance- Tinted Soft (Hydrophilic) Daily Wear Contact…Vizionfocus, Inc.2019—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199910
200210
201820
201910
202510
FIG. 1 — Lineage of K982997, 1995–2025Source: 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
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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
*K973063Frequency 55 (Methafilcon a) Hydrophilic Contact Lens for Daily Wear
Summary page 1
…) are substantially equivalent to FREQUENCY 55 (methafilcon A) Hydrophilic Contact Lenses for Daily Wear (clear and tinted) that received marketing clearance pursuant to K973063, currently marketed in the US. A comparison of properties is found in the chart below. Preclinical Testing The results of toxic…
Aspect Vision Care, Ltd.19971
†K971164Frequency 55 (Methafilcon a) Hydrophilic Contact LensAspect Vision Care, Ltd.1997—

Also cleared against K973063: 3 other devices →

What descends from it? (6)

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

NumberDeviceApplicantDecidedDescendants
K020392Frequency 55 UV (Methafilcon a) Soft (Hydrophlic) Contact Lens for Daily WearCooperVision, Inc.20023
K993252Methafilcon a Soft Hydrophilic Contact Lenses, Frequency 55, Frequency 55 UV (to BE…CooperVision, Inc.19991

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 4 years and passes through 2 companies; a new generation was cleared every 1.4 years on median.
  • 1 of the 4 ancestors has a recall of any class.
  • Of its descendants, K020392 (CooperVision, Inc., 2002) has gone furthest, with 3 descendants of its own.
  • 3 other devices also cite its predicate K973063.

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.

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?

The FREQUENCY™ 55 UV (methafilcon A) Hydrophilic Contact Lens (clear and tinted) is indicated for daily wear for the correction of refractive ametropia (myopia and hyperopia) and astigmatism in aphakic and not-aphakic persons with non-diseased eyes that may exhibit astigmatism up to 2.00 Diopters that does not interfere with visual acuity.

Eyecare practitioners may prescribe the lens for daily wear in a Frequent Replacement Program. The lenses may be disinfected using chemical or hydrogen peroxide disinfection systems.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K982997: Frequency 55 UV (Methafilcon a) Hydrophilic Contact Lens for Daily Wear (Clear and Tinted with UV Blocker).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K982997

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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