510(k) Report

510(k) · Cleared

Cleared

Endo-CHX

K070401510(k) TraditionalCleared Jul 11, 2007149-day reviewClass U

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

Essential Dental Systems, Inc. · KJJ Cleanser, Root Canal

Cleared on Jul 11, 2007 as substantially equivalent to K061689 (Puricore, Inc., 2006) and 1 other predicate after a 149-day review. Its family tree reaches back 4 generations to 2001. 2 later devices descend from it.

Decided
Jul 11, 2007
Review
149 days
Class
Class U
Product code
KJJ
Recalls
None
Predicates
2

Its longest line of descent runs back 4 generations to K003422 (2001). 6 ancestors in all, the oldest K962743 (1996). 2 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1999: 1 other ancestor1996: 1 other ancestor2011: 1 descendant cleared2016: 1 descendant clearedK003422 · Edta Root Canal Cleanser · Super Glide, Inc. · 2001K032361 · Endopure Root Canal Cleanser · Dentsply Intl. · 2004K053167 · Biopure Mtad Root Canal Cleanser · Dentsply Intl., Inc. · 2005K061689 · Aquatine EC Endodontic Cleanser · Puricore, Inc. · 20061995200020052010201520202025
Other ancestors, by generationDescendants, by generation 2 generations back: 2 other ancestors 1 generation forward: 1 descendant2 generations forward: 1 descendant K061689 · Aquatine EC Endodontic Cleanser · Puricore, Inc. · 2006K053167 · Biopure Mtad Root Canal Cleanser · Dentsply Intl., Inc. · 2005K032361 · Endopure Root Canal Cleanser · Dentsply Intl. · 2004K003422 · Edta Root Canal Cleanser · Super Glide, Inc. · 20010
  1. Root · 4 generations backK003422 Edta Root Canal CleanserSuper Glide, Inc. · 2001
  2. 3 generations backK032361 Endopure Root Canal CleanserDentsply Intl. · 2004
  3. 2 generations backK053167 Biopure Mtad Root Canal CleanserDentsply Intl., Inc. · 2005
  4. 1 generation backK061689 Aquatine EC Endodontic CleanserPuricore, Inc. · 2006
  5. This deviceK070401 Endo-CHXEssential Dental Systems, Inc. · 2007
  6. Descendant · cites it directly · 1 of its ownK112250 CHX=CHX PlusInter-Med, Inc. · 2011
  7. Descendant · 2 generations on · 0 of its ownK160577 PacEndo ChlorhexidinePac-Dent International, Inc. · 2016

Most influential descendants

Showing 2 of 2 · See all
  • K112250CHX=CHX PlusInter-Med, Inc. · 2011 · cites it directly1descendant
  • K160577PacEndo ChlorhexidinePac-Dent International, Inc. · 2016 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K003422Edta Root Canal CleanserSuper Glide, Inc.2001—
−3K032361Endopure Root Canal CleanserDentsply Intl.2004—
−2K053167Biopure Mtad Root Canal CleanserDentsply Intl., Inc.2005—
−1K061689Aquatine EC Endodontic CleanserPuricore, Inc.2006—
0 (this device)K070401Endo-CHXEssential Dental Systems, Inc.2007—
+1K112250CHX=CHX PlusInter-Med, Inc.2011—
+2K160577PacEndo ChlorhexidinePac-Dent International, Inc.2016—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199610
199910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201110
201610
FIG. 1 — Lineage of K070401, 2001–2016Source: 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 KJJ? 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 KJJ device

  1. #1 K241354 Sealer Solventscore 8.2 · 2 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? (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
*K061689Aquatine EC Endodontic Cleanser
Summary page 1
…duct Code and CFR Regulation Number: Unclassified, Product Code KJJ Classification Panel: Dental K061689, Aquatine T M EC Endodontic Cleanser, PuriCore, Inc.…
Puricore, Inc.2006—
*K053167Biopure Mtad Root Canal Cleanser
Summary page 1
…K061689, Aquatine T M EC Endodontic Cleanser, PuriCore, Inc. K053167, BioPureTM MTADTM Root Canal Cleanser, Predicate Device Names and 510(k) Dentsply International numbers: Device Description…
Dentsply Intl., Inc.2005—

Also cleared against K061689: 4 other devices →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K112250CHX=CHX PlusInter-Med, Inc.20111

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 6 years and passes through 5 companies; a new generation was cleared every 1.9 years on median.
  • None of the 6 ancestors has a recall.
  • Of its descendants, K112250 (Inter-Med, Inc., 2011) has gone furthest, with 1 descendant of its own.
  • 4 other devices also cite its predicate K061689.

How does its category compare?

All KJJ devices

KJJ Cleanser, Root Canal: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.

FDA decisions per year · KJJ

1in 2025

2007: 32009: 12011: 22013: 22014: 22015: 22016: 22017: 12018: 12020: 32021: 22024: 12025: 1
2007high 3 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KJJ

275in 2020

2007: 94 days median2020: 275 days median
2007high 275 (2020) · low 94 (2007)2026

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

Recalls per year · KJJ

7in 2019

2019: 7
2007high 7 (2019) · low 0 (2007)2026

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

Adverse event reports per year · KJJ

2in 2025

2007: 32013: 22014: 12015: 32016: 22018: 12019: 12020: 12023: 22025: 2
2007high 3 (2007) · low 0 (2008)2025

MAUDE reports naming product code KJJ, 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
200739403
20080—00
20091—00
20100—00
20112—00
20120—00
20132—02
20142—01
20152—03
20162—02
20171—00
20181—01
20190—71
2020327501
20212—00
20220—00
20230—02
20241—00
20251—02
20260—0—

What is it indicated for?

ENDO-CHXTM is intended to irrigate and cleanse root canal systems.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K070401: Endo-CHX.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K070401

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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