510(k) Report

510(k) · Cleared

Cleared

Argesol-WSF Pre-Solder for High Gold Dental Procelain Alloys

K942505510(k) TraditionalCleared Jun 16, 199421-day reviewClass II21 CFR 872.3060

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

Argen Precious Metals, Inc. · EJT Alloy, Gold-Based Noble Metal

Cleared on Jun 16, 1994 after a 21-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 2 later devices descend from it.

Decided
Jun 16, 1994
Review
21 days
Class
Class II
Product code
EJT
Recalls
None
Predicates
0

2 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2002: 1 descendant cleared2004: 1 descendant cleared1990200020102020
  1. This deviceK942505 Argesol-WSF Pre-Solder for High Gold Dental Procelain AlloysArgen Precious Metals, Inc. · 1994
  2. Descendant · cites it directly · 0 of its ownK040524 Porta Solder 1090 WWieland Dental + Technik GmbH & Co. KG · 2004
  3. Descendant · cites it directly · 0 of its ownK022470 Porta Solder 1080 WWieland Dental + Technik GmbH & Co. KG · 2002

Most influential descendants

Showing 2 of 2 · See all
  • K040524Porta Solder 1090 WWieland Dental + Technik GmbH & Co. KG · 2004 · cites it directly0descendants
  • K022470Porta Solder 1080 WWieland Dental + Technik GmbH & Co. KG · 2002 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K942505Argesol-WSF Pre-Solder for High Gold Dental Procelain AlloysArgen Precious Metals, Inc.1994—
+1K040524Porta Solder 1090 WWieland Dental + Technik GmbH & Co. KG2004—
+1K022470Porta Solder 1080 WWieland Dental + Technik GmbH & Co. KG2002—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200210
200410
FIG. 1 — Lineage of K942505, 1994–2004Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in EJT? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (2)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K040524Porta Solder 1090 WWieland Dental + Technik GmbH & Co. KG20040
K022470Porta Solder 1080 WWieland Dental + Technik GmbH & Co. KG20020

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?

  • Of its descendants, K040524 (Wieland Dental + Technik GmbH & Co. KG, 2004) has gone furthest, with 0 descendants of its own.

How does its category compare?

All EJT devices

EJT Alloy, Gold-Based Noble Metal: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · EJT

FDA has decided no EJT device since 2007.

Median 510(k) review, days · EJT

Too few EJT 510(k)s in any year since 2007 to give a median.

Recalls per year · EJT

No recall names EJT since 2007.

Adverse event reports per year · EJT

1in 2017

2011: 12014: 12016: 12017: 1
2007high 1 (2011) · low 0 (2007)2025

MAUDE reports naming product code EJT, 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
20070—00
20080—00
20090—00
20100—00
20110—01
20120—00
20130—00
20140—01
20150—00
20160—01
20170—01
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K942505: Argesol-WSF Pre-Solder for High Gold Dental Procelain Alloys.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K942505

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026