510(k) · Cleared

Cleared

Avante Z Zirconia (as)3 Blocks

K081749510(k) TraditionalCleared Sep 30, 2008103-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

Pentron Ceramics, Inc. · EIH Powder, Porcelain

Cleared on Sep 30, 2008 as substantially equivalent to K051705 (Ivoclar Vivadent, Inc., 2005) and 1 other predicate after a 103-day review. Its family tree reaches back 1 generation to 2005. 1 later device descends from it.

Decided: Sep 30, 2008
Review: 103 days
Class: Class II
Product code: EIH
Recalls: None
Predicates: 2

Its longest line of descent runs back 1 generation to K051705 (2005). 2 ancestors in all. 1 later device descends from it, 1 citing it directly.

By dateBy generation

Root · 1 generation backK051705 Ips E.Max Cad/Ips E.Max ZircadIvoclar Vivadent, Inc. · 2005 · Recalled
This deviceK081749 Avante Z Zirconia (as)3 BlocksPentron Ceramics, Inc. · 2008
Descendant · cites it directly · 0 of its ownK100232 Luminesse ZR BlanksTalladium, Inc. · 2010 · Recalled

Most influential descendants

Showing 1 of 1 · See all

K100232Luminesse ZR BlanksTalladium, Inc. · 2010 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K051705	Ips E.Max Cad/Ips E.Max Zircad	Ivoclar Vivadent, Inc.	2005	10
0 (this device)	K081749	Avante Z Zirconia (as)3 Blocks	Pentron Ceramics, Inc.	2008	—
+1	K100232	Luminesse ZR Blanks	Talladium, Inc.	2010	1

Other ancestors by year cleared

Year cleared	Devices	With a Class I recall
2007	1	0

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2010	1	0

FIG. 1 — Lineage of K081749, 2005–2010Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 K192231 Dental Glass Ceramics Blocksscore 15.2 · 3 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

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What was it cleared against? (2)

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.

Type	Number	Device	Applicant	Decided	Recalls
*	K051705	Ips E.Max Cad/Ips E.Max Zircad	Ivoclar Vivadent, Inc.	2005	10
*	K073108	Zeno ZR Disc Summary page 1 ….6660) Predicate Devices,: IPS e.max ZirCAD by Ivoclar Vivadent AG (KO51705) Zeno Zr Disc by Wie Iand Dental+Technik Gmbh&Co KG (K0731 08) Device Description: Avante Z Zirconia (A.,;) Blocks are partially sintered yttria- stabilized zirconia bli:…	Wieland Dental + Technik GmbH & Co. KG	2007	—

Also cleared against K051705: 20 other devices →

What descends from it? (1)

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

Number	Device	Applicant	Decided	Descendants
K100232	Luminesse ZR Blanks	Talladium, Inc.	2010	0

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?

1 of the 2 ancestors has a recall of any class.
Of its descendants, K100232 (Talladium, Inc., 2010) has gone furthest, with 0 descendants of its own.
20 other devices also cite its predicate K051705.

How does its category compare?

All EIH devices

EIH Powder, Porcelain: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · EIH

13in 2025

2007high 28 (2024) · low 9 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EIH

84in 2025

2007high 187 (2016) · low 63 (2007)2026

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

Recalls per year · EIH

1in 2025

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

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

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	15	63	0	0
2008	15	87	0	1
2009	15	79	0	0
2010	14	89	0	0
2011	14	80	0	1
2012	9	96	0	0
2013	16	107	0	6
2014	18	118	0	1
2015	23	118	0	0
2016	22	187	21	4
2017	16	149	0	1
2018	10	139	0	2
2019	16	125	0	1
2020	13	155	0	0
2021	17	131	0	22
2022	16	89	0	0
2023	15	114	0	0
2024	28	89	0	7
2025	13	84	1	1
2026	14	73	0	—

What is it indicated for?

Avante Z Zirconia (AS) 3 Blocks consists of machinable zirconia blocks for the preparation of full ceramic crowns, onlays. and multi-unit bridges and inlay bridges (anterior and molar).

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K081749 · printed Nov 4, 2026

Cite this page

510(k) Report. “K081749: Avante Z Zirconia (as)3 Blocks.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K081749

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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