510(k) Report

510(k) · Cleared

Cleared

Miele G 7781 Dental Thermal Disinfector

K950518510(k) TraditionalCleared Jan 26, 1996354-day reviewClass II21 CFR 880.6991

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

Miele Professional · LDS Device, Pasteurization, Hot Water

Cleared on Jan 26, 1996 after a 354-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Jan 26, 1996
Review
354 days
Class
Class II
Product code
LDS
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2003: 1 descendant cleared1995200020052010201520202025
  1. This deviceK950518 Miele G 7781 Dental Thermal DisinfectorMiele Professional · 1996
  2. Descendant · cites it directly · 0 of its ownK031799 Miele Dental Thermal Disinfector, Model G7881Miele, Inc. · 2003

Most influential descendants

Showing 1 of 1 · See all
  • K031799Miele Dental Thermal Disinfector, Model G7881Miele, Inc. · 2003 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K950518Miele G 7781 Dental Thermal DisinfectorMiele Professional1996—
+1K031799Miele Dental Thermal Disinfector, Model G7881Miele, Inc.2003—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200310
FIG. 1 — Lineage of K950518, 1996–2003Source: 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.

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  • Recall history across each candidate’s familyin the report
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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K031799Miele Dental Thermal Disinfector, Model G7881Miele, Inc.20030

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, K031799 (Miele, Inc., 2003) has gone furthest, with 0 descendants of its own.

How does its category compare?

All LDS devices

LDS Device, Pasteurization, Hot Water: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LDS

1in 2019

2019: 1
2007high 1 (2019) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LDS

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

Recalls per year · LDS

4in 2010

2010: 4
2007high 4 (2010) · low 0 (2007)2026

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

Adverse event reports per year · LDS

1in 2016

2007: 12009: 22010: 12011: 142012: 632013: 102015: 12016: 1
2007high 63 (2012) · low 0 (2008)2025

MAUDE reports naming product code LDS, 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—01
20080—00
20090—02
20100—41
20110—014
20120—063
20130—010
20140—00
20150—01
20160—01
20170—00
20180—00
20191—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K950518: Miele G 7781 Dental Thermal Disinfector.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K950518

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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