510(k) Report

510(k) · Cleared

Cleared

Signum composite flow; Signum universal bond; Signum metal bond ; Signum composite; Signum matrix; Signum liquid; Signum cre-active

K240660510(k) TraditionalCleared Sep 17, 2024193-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

Kulzer, LLC · EBF Material, Tooth Shade, Resin

Cleared on Sep 17, 2024 as substantially equivalent to K961434 (Vident, 1996) and 2 other predicates after a 193-day review. Its family tree reaches back 5 generations to 1990. 1 later device descends from it.

Decided
Sep 17, 2024
Review
193 days
Class
Class II
Product code
EBF
Recalls
None
Predicates
3

Its longest line of descent runs back 5 generations to K902115 (1990). 19 ancestors in all, the oldest K833757 (1984). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2021: 1 other ancestor1996: 4 other ancestors2013: 2 other ancestors1999: 1 other ancestor1997: 1 other ancestor1995: 1 other ancestor1991: 1 other ancestor1990: 2 other ancestors1984: 1 other ancestor2026: 1 descendant clearedK902115 · Palapress (R) Vario Resin · Kulzer, Inc. · 1990K972573 · Liqcrylic Pro Dental Resin · Dentsply Intl. · 1997×2: 2 generations cleared close together, K991220 (1999), K992645 (1999) K152373 · VITA VM LC Flow · Vita Zahnfabrik H.Rauter GmbH & Co. · 201519801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 2 other ancestors2 generations back: 2 other ancestors3 generations back: 6 other ancestors4 generations back: 4 other ancestors 1 generation forward: 1 descendant K152373 · VITA VM LC Flow · Vita Zahnfabrik H.Rauter GmbH & Co. · 2015K992645 · Sinfony · Espe Dental AG · 1999K991220 · Vitron H · Espe Dental AG · 1999K972573 · Liqcrylic Pro Dental Resin · Dentsply Intl. · 1997K902115 · Palapress (R) Vario Resin · Kulzer, Inc. · 1990−50
  1. Root · 5 generations backK902115 Palapress (R) Vario ResinKulzer, Inc. · 1990
  2. 4 generations backK972573 Liqcrylic Pro Dental ResinDentsply Intl. · 1997
  3. 3 generations backK991220 Vitron HEspe Dental AG · 1999
  4. 2 generations backK992645 SinfonyEspe Dental AG · 1999
  5. 1 generation backK152373 VITA VM LC FlowVita Zahnfabrik H.Rauter GmbH & Co. · 2015
  6. This deviceK240660 Signum composite flow; Signum universal bond; Signum metal bond…Kulzer, LLC · 2024
  7. Descendant · cites it directly · 0 of its ownK251587 VITA VMLC PrimerVita Zahnfabrik H. Rauter GmbH & Co. Kg. · 2026

Most influential descendants

Showing 1 of 1 · See all
  • K251587VITA VMLC PrimerVita Zahnfabrik H. Rauter GmbH & Co. Kg. · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K902115Palapress (R) Vario ResinKulzer, Inc.1990—
−4K972573Liqcrylic Pro Dental ResinDentsply Intl.1997—
−3K991220Vitron HEspe Dental AG1999—
−2K992645SinfonyEspe Dental AG1999—
−1K152373VITA VM LC FlowVita Zahnfabrik H.Rauter GmbH & Co.2015—
0 (this device)K240660Signum composite flow; Signum universal bond; Signum metal bond ; Signum…Kulzer, LLC2024—
+1K251587VITA VMLC PrimerVita Zahnfabrik H. Rauter GmbH & Co. Kg.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198410
199020
199110
199510
199640
199710
199910
201320
202110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K240660, 1990–2026Source: 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 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? (3)

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
*K961434Vita Zeta Crown and Bridge Acrylic Veneering System
Summary page 6
…r 872.3690 Product Code(s) EBF I Legally Marketed Predicate Devices 21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K961434 VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYg| | EBF K152373 VITA VM LC Flow EBF K211854 VITA Akzent LC EBD Device Description…
Vident1996—
*K152373VITA VM LC Flow
Summary page 6
…ces 21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K961434 VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYg| | EBF K152373 VITA VM LC Flow EBF K211854 VITA Akzent LC EBD Device Description Summary 21 CFR 807.92(a)(4) Signum Bondings (Signum metal bond…
Vita Zahnfabrik H.Rauter GmbH & Co.2015—
*K211854VITA Akzent LC
Summary page 6
…icate # Predicate Trade Name (Primary Predicate is listed first) Product Code K961434 VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYg| | EBF K152373 VITA VM LC Flow EBF K211854 VITA Akzent LC EBD Device Description Summary 21 CFR 807.92(a)(4) Signum Bondings (Signum metal bond, Signum universal bond) are…
Vita Zahnfabrik GmbH H Rauter & CO2021—

Also cleared against K961434: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K251587VITA VMLC PrimerVita Zahnfabrik H. Rauter GmbH & Co. Kg.20260

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 34 years and passes through 5 companies; a new generation was cleared every 7.1 years on median.
  • None of the 19 ancestors has a recall.
  • Of its descendants, K251587 (Vita Zahnfabrik H. Rauter GmbH & Co. Kg., 2026) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K961434.

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. 2024, this device’s year, is highlighted.

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?

Signum metal bond: - Bonding agent between framework surfaces made of metal alloys (precious metal, non-precious metal or titanium) and (meth-) acrylate-based veneering materials in conjunction with micromechanical retention. - Bonding agent between partial framework surfaces made of metal alloys (precious metal, non-precious metal or titanium) and (meth-) acrylate-based veneering materials or denture base materials (hot or auto-polymerizates). - Bonding…

Read the full statement (428 words)

Signum metal bond:

- Bonding agent between framework surfaces made of metal alloys (precious metal, non-precious metal or titanium) and (meth-) acrylate-based veneering materials in conjunction with micromechanical retention.

- Bonding agent between partial framework surfaces made of metal alloys (precious metal, non-precious metal or titanium) and (meth-) acrylate-based veneering materials or denture base materials (hot or auto-polymerizates).

- Bonding agent for extraoral repair of metal supported composite veneers.

Signum universal bond:

Metal

- Bonding agent between framework surfaces made of metal alloys (precious metal, non-precious metal or titanium) and (meth-) acrylate-based veneering materials in conjunction with macro-mechanical retentions.

- Bonding agent between partial framework surfaces made of metal alloys (precious metal, non-precious metal or titanium) and (meth-) acrylate-based veneering materials or denture base materials (hot or auto-polymerizates).

- Bonding agent for the extraoral repair of metal-supported composite veneers.

Zirconium dioxide

- Bonding agent between frameworks, implant abutments and single crowns made of ZrO2 and light-curing veneering materials.

- Bonding agent for the extraoral repair of composite veneers on ZrO2 frameworks.

High performance polymers (PEEK)

- Bonding agent between frameworks, implant abutments and individual crowns made of high performance polymers and light-curing veneering materials.

- Bonding agent between partial framework surfaces made of high-performance polymers and light-curing veneering materials or denture base materials (hot or auto-polymerizate).

- Bonding agent for the extraoral repair of composite veneers on PEEK frameworks.

Signum liquid:

For light-curing veneering materials from Kulzer:

- Restoring the dispersion layer of light curing veneering materials.

Signum composite / Signum composite flow / Signum matrix:

Suitable for veneering the following dental framework materials:

Metal alloys (precious metal, non-precious or titanium), zirconia, high-performance polymers (PEEK)

Suitable for partial alteration of the colour and shape of the following dental materials:

•PMMA

•Photopolymers

Suitable for the following prosthetic restorations:

•full and partial veneers for permanent framework-supported crowns and bridges

• veneering removable combination prosthetics (telescopic and tapered crowns and at-tachment prosthetics)

• veneering of superstructures/tertiary structures on implants

• metal-free front tooth and posterior tooth temporary restorations

• alteration of the colour and shape of Kulzer acrylic denture teeth

• alteration of the colour and shape of acrylic-based frameworks (PMMA).

• alteration of the colour and shape of Kulzer photopolymers that are approved for char-acterisation with Signum components (according to the photopolymer instructions for use)

Signum ere-active:

Individual characterization (e.g., of enamel cracks, white spots, imitation fillings, enamel wedges, intermediate colour layers, abrasion surfaces, fissures) of

•light-curing Kulzer veneering materials,

• Kulzer denture acrylic teeth and PMMA,

• (meth-)acrylate-based 3D printing photopolymers in accordance with the photopolymer instructions for use

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. “K240660: Signum composite flow; Signum universal bond; Signum metal bond ; Signum composite; Signum matrix; Signum liquid; Signum cre-active.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K240660

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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