510(k) Report

510(k) · Cleared

Cleared

Procera Allceram Bridge Material

K020269510(k) TraditionalCleared Mar 27, 200258-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

Procera Sandvik AB · EIH Powder, Porcelain

Cleared on Mar 27, 2002 as substantially equivalent to K983453 (Nobel Biocare Uas, Inc., 1998) after a 58-day review. Its family tree reaches back 2 generations to 1992.

Decided
Mar 27, 2002
Review
58 days
Class
Class II
Product code
EIH
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K920887 (1992). 3 ancestors in all. No later device cites it as a predicate yet.

Other ancestors, by year cleared 1992: 1 other ancestorK920887 · GDC-3338, Dental Solder Alloy · Deringer-Ney, Inc. · 1992K983453 · Procera Allceram Fusing Material · Nobel Biocare Uas, Inc. · 199819901992199419961998200020022004
Other ancestors, by generation 2 generations back: 1 other ancestor K983453 · Procera Allceram Fusing Material · Nobel Biocare Uas, Inc. · 1998K920887 · GDC-3338, Dental Solder Alloy · Deringer-Ney, Inc. · 19920
  1. Root · 2 generations backK920887 GDC-3338, Dental Solder AlloyDeringer-Ney, Inc. · 1992
  2. 1 generation backK983453 Procera Allceram Fusing MaterialNobel Biocare Uas, Inc. · 1998
  3. This deviceK020269 Procera Allceram Bridge MaterialProcera Sandvik AB · 2002
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K920887GDC-3338, Dental Solder AlloyDeringer-Ney, Inc.1992—
−1K983453Procera Allceram Fusing MaterialNobel Biocare Uas, Inc.1998—
0 (this device)K020269Procera Allceram Bridge MaterialProcera Sandvik AB2002—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199210
FIG. 1 — Lineage of K020269, 1992–2002Source: 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
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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
*K983453Procera Allceram Fusing Material
Summary page 1
…e Particles Trade Name: Procera® AllCeram Bridge Material Predicate Device: Substantial equivalence is claimed to Nobel Biocare AB’ Procera® AllCeram Fusing Material (K983453). Device Description: Procera ®All Ceram Bridge Material is composed of Procera® AllCeram Connection Material (a premixed suspe…
Nobel Biocare Uas, Inc.1998—

Also cleared against K983453: 1 other device →

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 10 years and passes through 3 companies; a new generation was cleared every 6.7 years on median.
  • None of the 3 ancestors has a recall.
  • 1 other device also cites its predicate K983453.

How does its category compare?

All EIH devices

EIH Powder, Porcelain: FDA decisions, review times, recalls and adverse event reports over 20 years.

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?

Procera® AllCeram Bridge Material is composed of Procera® AllCeram Connection Material (a premixed suspension of aluminium oxide particles, dispersant of the particles, binder of the particles and deionised water) and Procera® AllCeram Fusing Material (a suspension of glass material and water)

Procera® AllCeram Bridge Material is used to fuse together the sections of the core material in densely sintered aluminium oxide of a dental bridge.

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. “K020269: Procera Allceram Bridge Material.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K020269

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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