510(k) Report

510(k) · Cleared

Cleared

Venus Universal Light Curing Composite

K020131510(k) TraditionalCleared Feb 28, 200244-day reviewClass II21 CFR 872.3690

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

Heraeus Kulzer, Inc. · EBF Material, Tooth Shade, Resin

Cleared on Feb 28, 2002 after a 44-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 13 later devices descend from it.

Decided
Feb 28, 2002
Review
44 days
Class
Class II
Product code
EBF
Recalls
None
Predicates
0

13 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2004: 1 descendant cleared2015: 3 descendants cleared2007: 2 descendants cleared2011: 1 descendant cleared2010: 1 descendant cleared2017: 1 descendant cleared2021: 1 descendant cleared2019: 2 descendants cleared2009: 1 descendant cleared200020052010201520202025
  1. This deviceK020131 Venus Universal Light Curing CompositeHeraeus Kulzer, Inc. · 2002
  2. Descendant · cites it directly · 12 of its ownK042929 Estenia C&BKuraray Medical Kurashiki Plant · 2004
  3. Descendant · 2 generations on · 6 of its ownK111982 Clearfil DC Core PlusKuraray America, Inc. · 2011
  4. Descendant · 3 generations on · 4 of its ownK142625 PANAVIA SA Cement Plus Automix; (Universal (A2), White…Kuraray Noritake Dental, Inc. · 2015
  5. Descendant · 2 generations on · 4 of its ownK063595 Clearfil Majesty PosteriorKuraray America, Inc. · 2007
  6. Descendant · 2 generations on · 2 of its ownK150704 PANAVIA V5: Standard Kit (Universal (A2)), Standard Kit (Clear)…Kuraray Noritake Dental, Inc. · 2015

Showing 5 of 13 descendants. See all descendants

Descendants cleared per year

2004: 12007: 22009: 12010: 12011: 12015: 32017: 12019: 22021: 1
2004high 3 (2015) · low 0 (2005)2026

Most influential descendants

Showing 5 of 13 · See all
  • K042929Estenia C&BKuraray Medical Kurashiki Plant · 2004 · cites it directly12descendants
  • K111982Clearfil DC Core PlusKuraray America, Inc. · 2011 · 2 generations on6descendants
  • K142625PANAVIA SA Cement Plus Automix; (Universal (A2), White, Translucent); Value Pack…Kuraray Noritake Dental, Inc. · 2015 · 3 generations on4descendants
  • K063595Clearfil Majesty PosteriorKuraray America, Inc. · 2007 · 2 generations on4descendants
  • K150704PANAVIA V5: Standard Kit (Universal (A2)), Standard Kit (Clear), Introductory Kit…Kuraray Noritake Dental, Inc. · 2015 · 2 generations on2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K020131Venus Universal Light Curing CompositeHeraeus Kulzer, Inc.2002—
+1K042929Estenia C&BKuraray Medical Kurashiki Plant2004—
+2K111982Clearfil DC Core PlusKuraray America, Inc.2011—
+3K142625PANAVIA SA Cement Plus Automix; (Universal (A2), White, Translucent); Value…Kuraray Noritake Dental, Inc.2015—
+2K063595Clearfil Majesty PosteriorKuraray America, Inc.2007—
+2K150704PANAVIA V5: Standard Kit (Universal (A2)), Standard Kit (Clear), Introductory…Kuraray Noritake Dental, Inc.2015—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200410
200720
200910
201010
201110
201530
201710
201920
202110
FIG. 1 — Lineage of K020131, 2002–2021Source: 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 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in EBF? 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 EBF device

  1. #1 K202846 Tera Harzscore 18.5 · 7 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?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (13)

See all 13

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K042929Estenia C&BKuraray Medical Kurashiki Plant200412

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?

  • Of its descendants, K042929 (Kuraray Medical Kurashiki Plant, 2004) has gone furthest, with 12 descendants of its own.

How does its category compare?

All EBF devices

EBF Material, Tooth Shade, Resin: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · EBF

15in 2025

2007: 192008: 142009: 202010: 192011: 192012: 112013: 132014: 102015: 172016: 202017: 152018: 152019: 172020: 152021: 132022: 172023: 92024: 182025: 152026 (partial year): 16
2007high 20 (2009) · low 9 (2023)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EBF

43in 2025

2007: 49 days median2008: 79 days median2009: 84 days median2010: 75 days median2011: 81 days median2012: 86 days median2013: 153 days median2014: 112 days median2015: 123 days median2016: 205 days median2017: 108 days median2018: 115 days median2019: 159 days median2020: 190 days median2021: 178 days median2022: 63 days median2023: 87 days median2024: 120 days median2025: 43 days median2026 (partial year): 59 days median
2007high 205 (2016) · low 43 (2025)2026

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

Recalls per year · EBF

1in 2020

2007: 12008: 422009: 12010: 62011: 72017: 42019: 22020: 12026 (partial year): 2
2007high 42 (2008) · low 0 (2012)2026

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

Adverse event reports per year · EBF

1in 2025

2007: 62008: 102009: 82010: 312011: 312012: 622013: 2462014: 1952015: 1192016: 1432017: 422018: 82019: 112020: 22021: 22022: 22023: 82024: 52025: 1
2007high 246 (2013) · low 1 (2025)2025

MAUDE reports naming product code EBF, 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
2007194916
200814794210
2009208418
20101975631
20111981731
20121186062
2013131530246
2014101120195
2015171230119
2016202050143
201715108442
20181511508
201917159211
20201519012
20211317802
2022176302
202398708
20241812005
2025154301
202616592—

What is it indicated for?

Direct restoration of Class I-V cavities

Direct composite veneers

Shape corrections of teeth

Temporary splinting of teeth loosened by trauma or periodontal disease

Indirect restorations

Restoration of primary teeth

Core build-up

Temporary repairs of porcelain, composite

Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K020131: Venus Universal Light Curing Composite.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K020131

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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