510(k) Report

510(k) · Cleared

Cleared

Identium Heavy, Medium, Medium Soft, Light

K092867510(k) TraditionalCleared Oct 1, 200913-day reviewClass II21 CFR 872.3660

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

Kettenbach GmbH & Co. KG · ELW Material, Impression

Cleared on Oct 1, 2009 as substantially equivalent to K082560 (Kettenbach GmbH & Co. KG, 2008) and 3 other predicates after a 13-day review. Its family tree reaches back 5 generations to 1994. 1 later device descends from it.

Decided
Oct 1, 2009
Review
13 days
Class
Class II
Product code
ELW
Recalls
None
Predicates
4

Its longest line of descent runs back 5 generations to K943574 (1994). 11 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2005: 2 other ancestors2004: 1 other ancestor2002: 1 other ancestor1996: 1 other ancestor1997: 1 other ancestor2011: 1 descendant clearedK943574 · Capture Impression Material · Dentsply Intl. · 1994K973782 · Aquasil XLV Smart Wetting Impression Material · Dentsply Intl. · 1997K021410 · Aquasil Ultra XLV Smart Wetting Impression Material · Dentsply Intl. · 2002×2: 2 generations cleared close together, K082560 (2008), K083701 (2009) 1990200020102020
  1. Root · 5 generations backK943574 Capture Impression MaterialDentsply Intl. · 1994
  2. 4 generations backK973782 Aquasil XLV Smart Wetting Impression MaterialDentsply Intl. · 1997
  3. 3 generations backK021410 Aquasil Ultra XLV Smart Wetting Impression MaterialDentsply Intl. · 2002
  4. 2 generations backK082560 Panasil Impression Materials, Including Putty, Binetics, Tray…Kettenbach GmbH & Co. KG · 2008
  5. 1 generation backK083701 Panasil Initial Contact and Panasil TrayKettenbach GmbH & Co. KG · 2009
  6. This deviceK092867 Identium Heavy, Medium, Medium Soft, LightKettenbach GmbH & Co. KG · 2009
  7. Descendant · cites it directly · 0 of its ownK113279 Identium Heavy, Identium Medium, Identium Scan Heavy, Identium Scan…Kettenbach GmbH & Co. KG · 2011

Most influential descendants

Showing 1 of 1 · See all
  • K113279Identium Heavy, Identium Medium, Identium Scan Heavy, Identium Scan Medium, Identium…Kettenbach GmbH & Co. KG · 2011 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K943574Capture Impression MaterialDentsply Intl.1994—
−4K973782Aquasil XLV Smart Wetting Impression MaterialDentsply Intl.1997—
−3K021410Aquasil Ultra XLV Smart Wetting Impression MaterialDentsply Intl.2002—
−2K082560Panasil Impression Materials, Including Putty, Binetics, Tray, Monophase and…Kettenbach GmbH & Co. KG2008—
−1K083701Panasil Initial Contact and Panasil TrayKettenbach GmbH & Co. KG2009—
0 (this device)K092867Identium Heavy, Medium, Medium Soft, LightKettenbach GmbH & Co. KG2009—
+1K113279Identium Heavy, Identium Medium, Identium Scan Heavy, Identium Scan Medium…Kettenbach GmbH & Co. KG2011—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199610
199710
200210
200410
200520

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201110
FIG. 1 — Lineage of K092867, 1994–2011Source: 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 ELW? 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 ELW device

  1. #1 K254152 Dia-X Sil Light Bodyscore 14.1 · 8 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? (4)

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
*K082560Panasil Impression Materials, Including Putty, Binetics, Tray, Monophase and Contact
Summary page 1
…ssion (21 CFR 872.3660, Product Code: ELW) C. Predicate Devices Trade Name: Panasil® Impression Materials (K082560, K083701) Trade Names: GC Fusion/SENN and Fusion Fast Set/SENN…
Kettenbach GmbH & Co. KG2008—
*K083701Panasil Initial Contact and Panasil Tray
Summary page 1
…Product Code: ELW) C. Predicate Devices Trade Name: Panasil® Impression Materials (K082560, K083701) Trade Names: GC Fusion/SENN and Fusion Fast Set/SENN Impression Mat…
Kettenbach GmbH & Co. KG2009—
*K041398GC Fusion
Summary page 1
…K083701) Trade Names: GC Fusion/SENN and Fusion Fast Set/SENN Impression Materials (K041398, K043471) D. Device Description Identium®Impression Materials are addition-curing, elastomeric materials. Identium®Impres…
GC America, Inc.2004—
*K043471Fusion Fast
Summary page 1
…K083701) Trade Names: GC Fusion/SENN and Fusion Fast Set/SENN Impression Materials (K041398, K043471) D. Device Description Identium®Impression Materials are addition-curing, elastomeric materials. Identium®Impression Mate…
GC America, Inc.2005—

Also cleared against K082560: 4 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K113279Identium Heavy, Identium Medium, Identium Scan Heavy, Identium Scan Medium, Identium…Kettenbach GmbH & Co. KG20110

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 15 years and passes through 2 companies; a new generation was cleared every 3.3 years on median.
  • 1 of the 11 ancestors has a recall of any class.
  • Of its descendants, K113279 (Kettenbach GmbH & Co. KG, 2011) has gone furthest, with 0 descendants of its own.
  • 4 other devices also cite its predicate K082560.

How does its category compare?

All ELW devices

ELW Material, Impression: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · ELW

2in 2025

2007: 72008: 112009: 72010: 52011: 92012: 72013: 52014: 112015: 82016: 72017: 32018: 52019: 22020: 42021: 32022: 72023: 22024: 32025: 22026 (partial year): 3
2007high 11 (2008) · low 2 (2019)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ELW

98in 2024

2007: 60 days median2008: 30 days median2009: 43 days median2010: 88 days median2011: 83 days median2012: 87 days median2013: 67 days median2014: 122 days median2015: 93 days median2016: 166 days median2017: 89 days median2018: 126 days median2020: 99 days median2021: 76 days median2022: 60 days median2024: 98 days median2026 (partial year): 268 days median
2007high 268 (2026) · low 30 (2008)2026

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

Recalls per year · ELW

3in 2016

2010: 12012: 12013: 32016: 3
2007high 3 (2013) · low 0 (2007)2026

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

Adverse event reports per year · ELW

22in 2025

2007: 92008: 172009: 72010: 162011: 152012: 142013: 322014: 352015: 182016: 152017: 172018: 142019: 242020: 82021: 62022: 92023: 132024: 32025: 22
2007high 35 (2014) · low 3 (2024)2025

MAUDE reports naming product code ELW, 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
200776009
20081130017
200974307
2010588116
2011983015
2012787114
2013567332
201411122035
2015893018
20167166315
2017389017
20185126014
20192—024
202049908
202137606
202276009
20232—013
202439803
20252—022
202632680—

What is it indicated for?

Identium Light is to be used as a light-bodied, syringeable impression material in one-step technique (double mix) for: Impressions for Crowns/bridges, inlays/onlays and veneer preparations Reline impressions Impressions for full or partial dentures Identium Medium soft is to be used as a medium-bodied tray or syringeable impression material in one-step technique (monophase or double mix) for: Impressions for crowns/bridges, inlays/onlays and veneer…

Read the full statement (136 words)

Identium Light is to be used as a light-bodied, syringeable impression material in one-step technique (double mix) for:

Impressions for Crowns/bridges, inlays/onlays and veneer preparations

Reline impressions

Impressions for full or partial dentures

Identium Medium soft is to be used as a medium-bodied tray or syringeable impression material in one-step technique (monophase or double mix) for:

Impressions for crowns/bridges, inlays/onlays and veneer preparations

Functional impressions

Reline impressions

Identium Medium is to be used as a medium-bodied tray or syringeable impression material in one-step technique (monophase or double mix) for:

Impressions for crowns/bridges, inlays/onlays and veneer preparations

Implant impressions

Fixation impressions

Functional impressions

Identium Heavy is to be used as a heavy-bodied impression material in one-step technique (double mix) for:

Impressions for crowns/bridges, inlays/onlays and veneer preparations

Functional impressions

Impressions for full or partial dentures

Implant impressions

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K092867: Identium Heavy, Medium, Medium Soft, Light.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K092867

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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