510(k) Report

510(k) · Cleared

Cleared

Irrigation Tubing Set 2.2M and 3.8M

K041124510(k) TraditionalCleared Jun 7, 200439-day reviewClass I21 CFR 872.4200

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

W&H Dentalwerk Burmoos · EBW Controller, Foot, Handpiece And Cord

Cleared on Jun 7, 2004 after a 39-day review. The FDA summary names its predicate without a number. 1 later device descends from it.

Decided
Jun 7, 2004
Review
39 days
Class
Class I
Product code
EBW
Recalls
None
Predicates
0

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

Descendants, by year cleared 2009: 1 descendant cleared200020052010201520202025
  1. This deviceK041124 Irrigation Tubing Set 2.2M and 3.8MW&H Dentalwerk Burmoos · 2004
  2. Descendant · cites it directly · 0 of its ownK090727 Imm Dental Irrigation Tubing SetInnovative Medical Manufacturing Co. · 2009

Most influential descendants

Showing 1 of 1 · See all
  • K090727Imm Dental Irrigation Tubing SetInnovative Medical Manufacturing Co. · 2009 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K041124Irrigation Tubing Set 2.2M and 3.8MW&H Dentalwerk Burmoos2004—
+1K090727Imm Dental Irrigation Tubing SetInnovative Medical Manufacturing Co.2009—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
FIG. 1 — Lineage of K041124, 2004–2009Source: 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 EBW? 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 EBW device

  1. #1 K251701 Star E900 Electric Systemscore 12.2 · 6 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? (1)

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
*—Irrigation tubings, which were part (accessory) of the submissions of the dental…
Named without a submission number
—

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K090727Imm Dental Irrigation Tubing SetInnovative Medical Manufacturing Co.20090

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, K090727 (Innovative Medical Manufacturing Co., 2009) has gone furthest, with 0 descendants of its own.

How does its category compare?

All EBW devices

EBW Controller, Foot, Handpiece And Cord: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · EBW

3in 2025

2009: 52010: 12011: 32012: 12013: 12014: 32015: 12016: 12017: 42018: 12019: 22020: 12021: 22022: 62024: 42025: 32026 (partial year): 3
2007high 6 (2022) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EBW

220in 2025

2009: 112 days median2011: 226 days median2014: 189 days median2017: 227 days median2022: 479 days median2024: 268 days median2025: 220 days median2026 (partial year): 269 days median
2007high 479 (2022) · low 112 (2009)2026

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

Recalls per year · EBW

1in 2013

2013: 1
2007high 1 (2013) · low 0 (2007)2026

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

Adverse event reports per year · EBW

13in 2025

2009: 162010: 182011: 12012: 52013: 12014: 42015: 132016: 62017: 132018: 462019: 552020: 712021: 572022: 312023: 172024: 142025: 13
2007high 71 (2020) · low 0 (2007)2025

MAUDE reports naming product code EBW, 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
20095112016
20101—018
2011322601
20121—05
20131—11
2014318904
20151—013
20161—06
20174227013
20181—046
20192—055
20201—071
20212—057
20226479031
20230—017
20244268014
20253220013
202632690—

What is it indicated for?

The irrigation tubing set is an accessory to dental

surgical units.

The irrigation tubing set is used to supply treatment

fluid/coolant liquid from the reservoir to the handpiece

via a pump

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K041124: Irrigation Tubing Set 2.2M and 3.8M.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K041124

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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