510(k) Report

510(k) · Cleared

Cleared

Aquasil Easy Mix Putty Impression Material

K973781510(k) TraditionalCleared Dec 11, 199769-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

Dentsply Intl. · ELW Material, Impression

Cleared on Dec 11, 1997 as substantially equivalent to K781151 (Dentsply Intl., 1978) and 1 other predicate after a 69-day review. Its family tree reaches back 1 generation to 1978. 1 later device descends from it.

Decided
Dec 11, 1997
Review
69 days
Class
Class II
Product code
ELW
Recalls
None
Predicates
2

Its longest line of descent runs back 1 generation to K781151 (1978). 2 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1994: 1 other ancestor2006: 1 descendant clearedK781151 · Reprosil · Dentsply Intl. · 197819801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor 1 generation forward: 1 descendant K781151 · Reprosil · Dentsply Intl. · 19780
  1. Root · 1 generation backK781151 ReprosilDentsply Intl. · 1978
  2. This deviceK973781 Aquasil Easy Mix Putty Impression MaterialDentsply Intl. · 1997
  3. Descendant · cites it directly · 0 of its ownK061427 Pre-Impression Conditioning SolutionDentsply Intl. · 2006

Most influential descendants

Showing 1 of 1 · See all
  • K061427Pre-Impression Conditioning SolutionDentsply Intl. · 2006 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K781151ReprosilDentsply Intl.1978—
0 (this device)K973781Aquasil Easy Mix Putty Impression MaterialDentsply Intl.1997—
+1K061427Pre-Impression Conditioning SolutionDentsply Intl.2006—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200610
FIG. 1 — Lineage of K973781, 1978–2006Source: 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
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K781151Reprosil
Summary page 1
…eptember 19, 1997 TRADE NAME: AQUASIL™ EASY MIX PUTTY IMPRESSION MATERIAL CLASSIFICATION NAME: Impression Material PREDICATE DEVICE: Reprosil® Putty Impression Material K781151A Aquasil Smart Wetting® Impression Material K943574 DEVICE DESCRIPTION: AQUASIL EASY MIX PUTTY IMPRESSION MATERIAL is a very hig…
Dentsply Intl.1978—
*K943574Capture Impression Material
Summary page 1
…Y IMPRESSION MATERIAL CLASSIFICATION NAME: Impression Material PREDICATE DEVICE: Reprosil® Putty Impression Material K781151A Aquasil Smart Wetting® Impression Material K943574 DEVICE DESCRIPTION: AQUASIL EASY MIX PUTTY IMPRESSION MATERIAL is a very high viscosity, elastomeric impression material with ex…
Dentsply Intl.1994—

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K061427Pre-Impression Conditioning SolutionDentsply Intl.20060

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?

  • None of the 2 ancestors has a recall.
  • Of its descendants, K061427 (Dentsply Intl., 2006) has gone furthest, with 0 descendants of its own.

How does its category compare?

All ELW devices

ELW Material, Impression: FDA decisions, review times, recalls and adverse event reports over 20 years.

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?

AQUASIL EASY MIX PUTTY IMPRESSION MATERIAL is used as a tray material in a dual phase impression Technique. It is designed for taking multiple unit impressions of teeth and/or oral tissue.

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. “K973781: Aquasil Easy Mix Putty Impression Material.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K973781

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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