510(k) Report

510(k) · Cleared

Cleared

Eds Combo-Rinse

K140846510(k) TraditionalCleared Jul 25, 2014113-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 25, 2014 as substantially equivalent to K103244 (Dentsply Intl., Inc., 2011) and 2 other predicates after a 113-day review. Its family tree reaches back 4 generations to 2001.

Decided
Jul 25, 2014
Review
113 days
Class
Class U
Product code
KJJ
Recalls
None
Predicates
3

Its longest line of descent runs back 4 generations to K003422 (2001). 7 ancestors in all, the oldest K923842 (1992). No later device cites it as a predicate yet.

  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 backK103244 Qmix 2IN1 Endodontic Irrigating SolutionDentsply Intl., Inc. · 2011
  5. This deviceK140846 Eds Combo-RinseEssential Dental Systems, Inc. · 2014
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—
−1K103244Qmix 2IN1 Endodontic Irrigating SolutionDentsply Intl., Inc.2011—
0 (this device)K140846Eds Combo-RinseEssential Dental Systems, Inc.2014—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199210
199510
201010
FIG. 1 — Lineage of K140846, 2001–2014Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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? (3)

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
*K103244Qmix 2IN1 Endodontic Irrigating Solution
Summary page 1
…Device class: Unclassified Product Code: KJJ 3. Predicate Device Information: 1. QMixTM 2inl Endodontic Irrigating Solution, Dentsply International, K1 03244 2. Etch-37TM, Bisco Inc., K101485 3. MicroPrime B, Danville Engineering Inc., K953504 4. Device Description:…
Dentsply Intl., Inc.2011—
*K101485All-Etch, All- Etch with Bac; Uni- Etch, Uni- Etch with Bac; Etch- 37, Etch- 37 with…
Summary page 1
…ct Code: KJJ 3. Predicate Device Information: 1. QMixTM 2inl Endodontic Irrigating Solution, Dentsply International, K1 03244 2. Etch-37TM, Bisco Inc., K101485 3. MicroPrime B, Danville Engineering Inc., K953504 4. Device Description: EDS Combo-Rinse is an aqueous soluti…
Bisco, Inc.2010—
*K953504Microprime
Summary page 1
…QMixTM 2inl Endodontic Irrigating Solution, Dentsply International, K1 03244 2. Etch-37TM, Bisco Inc., K101485 3. MicroPrime B, Danville Engineering Inc., K953504 4. Device Description: EDS Combo-Rinse is an aqueous solution for use during the irrigation phase of endodontic…
Danville Engineering, Inc.1995—

Also cleared against K103244: 3 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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 13 years and passes through 4 companies; a new generation was cleared every 3.4 years on median.
  • None of the 7 ancestors has a recall.
  • 3 other devices also cite its predicate K103244.

How does its category compare?

All KJJ devices

KJJ Cleanser, Root Canal: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, 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?

EDS Combo-Rinse is intended to cleanse root canal systems by irrigating root canals.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K140846: Eds Combo-Rinse.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K140846

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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