510(k) Report

510(k) · Cleared

Cleared

Naturelle Daily Disposable (Hilafilcon B) Cosmetically Tinted Contact Lens

K112192510(k) SpecialCleared Oct 25, 201188-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

Bausch & Lomb, Inc. · MVN Lens, Contact, (Disposable)

Cleared on Oct 25, 2011 as substantially equivalent to K061157 (Bausch & Lomb, 2006) after an 88-day review. Its family tree reaches back 4 generations to 1998.

Decided
Oct 25, 2011
Review
88 days
Class
Class II
Product code
MVN
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K974780 (1998). 5 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 4 generations backK974780 Soflens (TM) One Day Disposable (Hilafilcon a) Visibility Tinted…Bausch & Lomb, Inc. · 1998
  2. 3 generations backK983894 Bausch & Lomb Phoenix (Hilafilcon a) Visibility Tinted Contact LensBausch & Lomb, Inc. · 1998
  3. 2 generations backK994125 Bausch & Lomb 2-Week (Hilafilcon B) Visibility Tinted Contact LensesBausch & Lomb, Inc. · 2000
  4. 1 generation backK061157 Soflens One Day Plus Disposable (Hilafilcon B) Visibility Tinted…Bausch & Lomb · 2006
  5. This deviceK112192 Naturelle Daily Disposable (Hilafilcon B) Cosmetically Tinted…Bausch & Lomb, Inc. · 2011
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K974780Soflens (TM) One Day Disposable (Hilafilcon a) Visibility Tinted Contact LensBausch & Lomb, Inc.1998—
−3K983894Bausch & Lomb Phoenix (Hilafilcon a) Visibility Tinted Contact LensBausch & Lomb, Inc.1998—
−2K994125Bausch & Lomb 2-Week (Hilafilcon B) Visibility Tinted Contact LensesBausch & Lomb, Inc.2000—
−1K061157Soflens One Day Plus Disposable (Hilafilcon B) Visibility Tinted Contact LensBausch & Lomb2006—
0 (this device)K112192Naturelle Daily Disposable (Hilafilcon B) Cosmetically Tinted Contact LensBausch & Lomb, Inc.2011—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200110
FIG. 1 — Lineage of K112192, 1998–2011Source: 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 MVN? 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 MVN device

  1. #1 K261812 HOYA Illumina (sorafilcon A) Daily Disposable…score 14.0 · 9 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
*K061157Soflens One Day Plus Disposable (Hilafilcon B) Visibility Tinted Contact Lens
Summary page 1
…925 (b) (1)) Trade Name: 3.0 Predicate Device The predicate device is Bausch & Lomb SofLens® Daily Disposable (hilafiicon B) Visibility Tinted Contact Lens cleared in K061157 on June 22, 2006. 4.0 Device Description The Bausch + Lomb Naturelle Cosmetically Tinted daily disposable (hilafilcon B) Contac…
Bausch & Lomb2006—

Also cleared against K061157: 2 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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 13 years and passes through 2 companies; a new generation was cleared every 5.3 years on median.
  • None of the 5 ancestors has a recall.
  • 2 other devices also cite its predicate K061157.

How does its category compare?

All MVN devices

MVN Lens, Contact, (Disposable): FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · MVN

2in 2020

2007: 12008: 22011: 12013: 12015: 22020: 22026 (partial year): 1
2007high 2 (2008) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MVN

Too few MVN 510(k)s in any year since 2007 to give a median.

Recalls per year · MVN

2in 2013

2009: 12011: 12013: 22026 (partial year): 1
2007high 2 (2013) · low 0 (2007)2026

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

Adverse event reports per year · MVN

22in 2025

2010: 32011: 92012: 252013: 352014: 202015: 102016: 182017: 232018: 322019: 342020: 322021: 242022: 182023: 242024: 252025: 22
2007high 35 (2013) · low 0 (2007)2025

MAUDE reports naming product code MVN, 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
20071—00
20082—00
20090—10
20100—03
20111—19
20120—025
20131—235
20140—020
20152—010
20160—018
20170—023
20180—032
20190—034
20202—032
20210—024
20220—018
20230—024
20240—025
20250—022
20261—1—

What is it indicated for?

The Bausch + Lomb Naturelle Daily Disposable (hilafilcon B) Cosmetically Tinted Contact Lens is indicated for the daily wear correction of refractive ametropia (myopia and hyperopia) in aphakic and not-aphakic persons with non-diseased eyes, exhibiting astigmatism of 2.00 diopters or less, that does not interfere with visual acuity. The lens may be prescribed in spherical powers ranging from +20.00D to -20.00D.

The lens is to be prescribed for single-use disposable wear, and is to be discarded after each removal.

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. “K112192: Naturelle Daily Disposable (Hilafilcon B) Cosmetically Tinted Contact Lens.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K112192

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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