510(k) Report

510(k) · Cleared

Cleared

V-Mix

K193357510(k) TraditionalCleared Oct 23, 2020324-day reviewClass U

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

Inter-Med/Vista Dental Products · KJJ Cleanser, Root Canal

Cleared on Oct 23, 2020 as substantially equivalent to K082470 (Inter-Med, Inc., 2009) and 2 other predicates after a 324-day review. Its family tree reaches back 5 generations to 2001. 1 later device descends from it.

Decided
Oct 23, 2020
Review
324 days
Class
Class U
Product code
KJJ
Recalls
None
Predicates
3

Its longest line of descent runs back 5 generations to K003422 (2001). 13 ancestors in all, the oldest K950365 (1995). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2020: 1 other ancestor2016: 1 other ancestor2011: 1 other ancestor1996: 1 other ancestor2007: 1 other ancestor1999: 1 other ancestor2003: 1 other ancestor1995: 1 other ancestor2021: 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. · 2006K082470 · Sodium Hypochlorite 3 & 6% Solution and 6% with Wetting Agents to Lower Surface Tension Marketed as Chlor-Xtra · Inter-Med, Inc. · 2009 · recalled1995200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 3 other ancestors3 generations back: 2 other ancestors4 generations back: 2 other ancestors 1 generation forward: 1 descendant K082470 · Sodium Hypochlorite 3 & 6% Solution and 6% with Wetting Agents to Lower Surface Tension Marketed as Chlor-Xtra · Inter-Med, Inc. · 2009 · recalledK061689 · 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. · 2001−50
  1. Root · 5 generations backK003422 Edta Root Canal CleanserSuper Glide, Inc. · 2001
  2. 4 generations backK032361 Endopure Root Canal CleanserDentsply Intl. · 2004
  3. 3 generations backK053167 Biopure Mtad Root Canal CleanserDentsply Intl., Inc. · 2005
  4. 2 generations backK061689 Aquatine EC Endodontic CleanserPuricore, Inc. · 2006
  5. 1 generation backK082470 Sodium Hypochlorite 3 & 6% Solution and 6% with Wetting Agents to…Inter-Med, Inc. · 2009 · Recalled
  6. This deviceK193357 V-MixInter-Med/Vista Dental Products · 2020
  7. Descendant · cites it directly · 0 of its ownK211813 TritonInter-Med / Vista Dental · 2021

Most influential descendants

Showing 1 of 1 · See all
  • K211813TritonInter-Med / Vista Dental · 2021 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K003422Edta Root Canal CleanserSuper Glide, Inc.2001—
−4K032361Endopure Root Canal CleanserDentsply Intl.2004—
−3K053167Biopure Mtad Root Canal CleanserDentsply Intl., Inc.2005—
−2K061689Aquatine EC Endodontic CleanserPuricore, Inc.2006—
−1K082470Sodium Hypochlorite 3 & 6% Solution and 6% with Wetting Agents to Lower…Inter-Med, Inc.20097
0 (this device)K193357V-MixInter-Med/Vista Dental Products2020—
+1K211813TritonInter-Med / Vista Dental2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
199610
199910
200310
200710
201110
201610
202010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202110
FIG. 1 — Lineage of K193357, 2001–2021Source: 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? (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
*K082470Sodium Hypochlorite 3 & 6% Solution and 6% with Wetting Agents to Lower Surface Tension…
Summary page 4
…ame Proprietary Name: V-Mix Common Name: Cleanser, Root Canal Product Code: KJJ Device Class: Unclassified 3. Predicate Devices Chlor-Xtra (K082470) by Inter-Med / Vista Dental Products o Common Name: Cleanser, Root Canal o Product Code: KJJ o Device Cl…
Inter-Med, Inc.20097
*K053167Biopure Mtad Root Canal Cleanser
Summary page 4
…ista Dental Products o Common Name: Cleanser, Root Canal o Product Code: KJJ o Device Class: Unclassified Biopure MTAD Root Canal Cleanser (K053167) by Dentsply o Common Name: Cleanser, Root Canal o Product Code: KJJ o Device Class: Unclassified V…
Dentsply Intl., Inc.2005—
*K193409Vista Rinse, Vista Rinse Plus
Cleared while this submission was under review
Summary page 4
…Canal Cleanser (K053167) by Dentsply o Common Name: Cleanser, Root Canal o Product Code: KJJ o Device Class: Unclassified Vista Rinse Plus (K193409) by Inter-Med / Vista Dental Products o Common Name: Cleanser, Root Canal o Product Code: KJJ o Device Cl…
Inter-Med/Vista Dental Products2020—

Also cleared against K082470: 4 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K211813TritonInter-Med / Vista Dental20210

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 19 years and passes through 6 companies; a new generation was cleared every 2.6 years on median.
  • 1 of the 13 ancestors has a recall of any class.
  • Of its descendants, K211813 (Inter-Med / Vista Dental, 2021) has gone furthest, with 0 descendants of its own.
  • 4 other devices also cite its predicate K082470.

How does its category compare?

All KJJ devices

KJJ Cleanser, Root Canal: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, 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?

V-Mix is used for debridement, removing the smear layer, and cleansing the root canal system.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K193357: V-Mix.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K193357

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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