510(k) Report

510(k) · Cleared

Cleared

BruxZir Opaque Coloring Liquid

K220960510(k) TraditionalCleared Jun 29, 202289-day reviewClass II21 CFR 872.6660

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

Prismatik Dentalcraft, Inc. · EIH Powder, Porcelain

Cleared on Jun 29, 2022 as substantially equivalent to K190518 (Zirkonzahn Srl, 2019) after an 89-day review. Its family tree reaches back 4 generations to 2001. 1 later device descends from it.

Decided
Jun 29, 2022
Review
89 days
Class
Class II
Product code
EIH
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K011394 (2001). 1 later device descends from it, 1 citing it directly.

  1. Root · 4 generations backK011394 Lava Frame, Lava Frame Shade, Lava CeramEspe Dental AG · 2001
  2. 3 generations backK111257 Heisenberg Dyeing Liquids3M Espe AG · 2011
  3. 2 generations backK182833 ArgenZ Liquid Shade, ArgenZ Incisal Effect, ArgenZ Color Modifier…The Argen Corporation · 2019
  4. 1 generation backK190518 Color Liquid, Vita LiquidZirkonzahn Srl · 2019
  5. This deviceK220960 BruxZir Opaque Coloring LiquidPrismatik Dentalcraft, Inc. · 2022
  6. Descendant · cites it directly · 0 of its ownK231347 BruxZir™ TintEFX Coloring LiquidPrismatik Dentalcraft, Inc. · 2023

Most influential descendants

Showing 1 of 1 · See all
  • K231347BruxZir™ TintEFX Coloring LiquidPrismatik Dentalcraft, Inc. · 2023 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K011394Lava Frame, Lava Frame Shade, Lava CeramEspe Dental AG2001—
−3K111257Heisenberg Dyeing Liquids3M Espe AG2011—
−2K182833ArgenZ Liquid Shade, ArgenZ Incisal Effect, ArgenZ Color Modifier, ArgenZ…The Argen Corporation2019—
−1K190518Color Liquid, Vita LiquidZirkonzahn Srl2019—
0 (this device)K220960BruxZir Opaque Coloring LiquidPrismatik Dentalcraft, Inc.2022—
+1K231347BruxZir™ TintEFX Coloring LiquidPrismatik Dentalcraft, Inc.2023—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
FIG. 1 — Lineage of K220960, 2001–2023Source: 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 EIH? 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 EIH device

  1. #1 K192231 Dental Glass Ceramics Blocksscore 15.2 · 3 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
*K190518Color Liquid, Vita Liquid
Summary page 4
…Regulatory Class: Class II Product Code: EIH III. PRIMARY PREDICATE DEVICE Zirkonzahn COLOUR LIQUID (K190518) IV. DEVICE DESCRIPTION BruxZir™ Opaque Coloring Liquid comprises a set of solutions that enhanc…
Zirkonzahn Srl2019—

Also cleared against K190518: 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
K231347BruxZir™ TintEFX Coloring LiquidPrismatik Dentalcraft, Inc.20230

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 21 years and passes through 5 companies; a new generation was cleared every 7.7 years on median.
  • None of the 4 ancestors has a recall.
  • Of its descendants, K231347 (Prismatik Dentalcraft, Inc., 2023) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K190518.

How does its category compare?

All EIH devices

EIH Powder, Porcelain: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · EIH

13in 2025

2007: 152008: 152009: 152010: 142011: 142012: 92013: 162014: 182015: 232016: 222017: 162018: 102019: 162020: 132021: 172022: 162023: 152024: 282025: 132026 (partial year): 14
2007high 28 (2024) · low 9 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EIH

84in 2025

2007: 63 days median2008: 87 days median2009: 79 days median2010: 89 days median2011: 80 days median2012: 96 days median2013: 107 days median2014: 118 days median2015: 118 days median2016: 187 days median2017: 149 days median2018: 139 days median2019: 125 days median2020: 155 days median2021: 131 days median2022: 89 days median2023: 114 days median2024: 89 days median2025: 84 days median2026 (partial year): 73 days median
2007high 187 (2016) · low 63 (2007)2026

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

Recalls per year · EIH

1in 2025

2016: 212025: 1
2007high 21 (2016) · low 0 (2007)2026

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

Adverse event reports per year · EIH

1in 2025

2008: 12011: 12013: 62014: 12016: 42017: 12018: 22019: 12021: 222024: 72025: 1
2007high 22 (2021) · low 0 (2007)2025

MAUDE reports naming product code EIH, 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
2007156300
2008158701
2009157900
2010148900
2011148001
201299600
20131610706
20141811801
20152311800
201622187214
20171614901
20181013902
20191612501
20201315500
202117131022
2022168900
20231511400
2024288907
2025138411
202614730—

What is it indicated for?

BruxZir™ Opaque Coloring Liquid is used for coloring pre-sintered zirconia structures.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K220960: BruxZir Opaque Coloring Liquid.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K220960

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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