510(k) Report

510(k) · Cleared

Cleared

Prettau Anterior T0

K151490510(k) TraditionalCleared Oct 8, 2015127-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

Zirkonzahn GmbH · EIH Powder, Porcelain

Cleared on Oct 8, 2015 as substantially equivalent to K132230 (Zirkonzahn Srl, 2014) after a 127-day review. Its family tree reaches back 2 generations to 2006.

Decided
Oct 8, 2015
Review
127 days
Class
Class II
Product code
EIH
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K061851 (2006). No later device cites it as a predicate yet.

K061851 · Zirkonzahn Ice · Zirkonzahn GmbH · 2006K132230 · Ice Zirkon Transluzent · Zirkonzahn Srl · 2014200620082010201220142016
  1. Root · 2 generations backK061851 Zirkonzahn IceZirkonzahn GmbH · 2006
  2. 1 generation backK132230 Ice Zirkon TransluzentZirkonzahn Srl · 2014
  3. This deviceK151490 Prettau Anterior T0Zirkonzahn GmbH · 2015
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K061851Zirkonzahn IceZirkonzahn GmbH2006—
−1K132230Ice Zirkon TransluzentZirkonzahn Srl2014—
0 (this device)K151490Prettau Anterior T0Zirkonzahn GmbH2015—
FIG. 1 — Lineage of K151490, 2006–2015Source: 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
*K132230Ice Zirkon Transluzent
Summary page 4
…use, Class II Product Code: EIH Panel: Dental LEGALLY MARKETED DEVICE (PREDICATE DEVICE) ICE Zirkon Transluzen Plus (K132230) by Zirkonzahn Srl INTENDED USE: PRETTAU® ANTERIOR T0 is intended to be used for the manufacturing of metal free single-unit…
Zirkonzahn Srl2014—

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 9 years and passes through 2 companies; a new generation was cleared every 8.1 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All EIH devices

EIH Powder, Porcelain: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, 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?

PRETTAU® ANTERIOR TO is intended to be used for the manufacturing of metal free single-unit anterior and posterior

prostheses, inlays, onlays, veneers bonded dental restorations.

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. “K151490: Prettau Anterior T0.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K151490

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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