510(k) Report

510(k) · Cleared

Cleared

Dbswin, Vistaeasy

K203287510(k) SpecialCleared Nov 18, 20209-day reviewClass II21 CFR 892.2050

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

Dürr Dental SE · LLZ System, Image Processing, Radiological

Cleared on Nov 18, 2020 as substantially equivalent to K190629 (Durr Dental SE, 2019) after a 9-day review. Its family tree reaches back 7 generations to 1993.

Decided
Nov 18, 2020
Review
9 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K930527 (1993). 8 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 7 generations backK930527 Dental LinkEscan, Inc. · 1993
  2. 6 generations backK955237 Tigerscan/TigerviewTau Corp. · 1996
  3. 5 generations backK061035 Tigerview ProfessionalTelevere Systems · 2006
  4. 4 generations backK082623 Visix ImagingTelevere Systems · 2009
  5. 3 generations backK143290 DBSWIN and VistaEasy Imaging SoftwareDurr Dental AG · 2016
  6. 2 generations backK161444 DBSWIN and VistaEasy Imaging SoftwareDuerr Dental AG · 2016
  7. 1 generation backK190629 DBSWIN and VISTAEASY Imaging SoftwareDurr Dental SE · 2019
  8. This deviceK203287 Dbswin, VistaeasyDürr Dental SE · 2020
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K930527Dental LinkEscan, Inc.1993—
−6K955237Tigerscan/TigerviewTau Corp.1996—
−5K061035Tigerview ProfessionalTelevere Systems2006—
−4K082623Visix ImagingTelevere Systems2009—
−3K143290DBSWIN and VistaEasy Imaging SoftwareDurr Dental AG2016—
−2K161444DBSWIN and VistaEasy Imaging SoftwareDuerr Dental AG2016—
−1K190629DBSWIN and VISTAEASY Imaging SoftwareDurr Dental SE2019—
0 (this device)K203287Dbswin, VistaeasyDürr Dental SE2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199810
FIG. 1 — Lineage of K203287, 1993–2020Source: 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 LLZ? 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 LLZ device

  1. #1 K230955 syngo Application Softwarescore 21.5 · 11 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
*K190629DBSWIN and VISTAEASY Imaging Software
Summary page 5
…892.2050 Device Class 2 4. Legally Marketed Predicate Device Information: 510(k) Number: K190629 Manufacturer: "DÜRR DENTAL SE". Trade /Proprietary Name DBSWIN and VistaEasy Imagin…
Durr Dental SE2019—

Also cleared against K190629: 1 other device →

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 27 years and passes through 7 companies; a new generation was cleared every 2.8 years on median.
  • None of the 8 ancestors has a recall.
  • 1 other device also cites its predicate K190629.

How does its category compare?

All LLZ devices

LLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · LLZ

58in 2025

2007: 762008: 942009: 702010: 512011: 1062012: 822013: 952014: 782015: 642016: 822017: 782018: 1042019: 742020: 812021: 832022: 652023: 872024: 622025: 582026 (partial year): 45
2007high 106 (2011) · low 51 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LLZ

173in 2025

2007: 36 days median2008: 52 days median2009: 62 days median2010: 98 days median2011: 79 days median2012: 87 days median2013: 84 days median2014: 89 days median2015: 90 days median2016: 90 days median2017: 107 days median2018: 105 days median2019: 107 days median2020: 115 days median2021: 116 days median2022: 137 days median2023: 157 days median2024: 131 days median2025: 173 days median2026 (partial year): 110 days median
2007high 173 (2025) · low 36 (2007)2026

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

Recalls per year · LLZ

11in 2025

2007: 202008: 322009: 212010: 172011: 302012: 122013: 642014: 62015: 162016: 122017: 52018: 72019: 22020: 62021: 32022: 42023: 82024: 62025: 112026 (partial year): 14
2007high 64 (2013) · low 2 (2019)2026

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

Adverse event reports per year · LLZ

116in 2025

2007: 1522008: 1542009: 1452010: 1452011: 4542012: 2662013: 1,1302014: 15,6312015: 2112016: 2902017: 1042018: 722019: 882020: 822021: 702022: 282023: 262024: 422025: 116
2007high 15,631 (2014) · low 26 (2023)2025

MAUDE reports naming product code LLZ, 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
2007763620152
2008945232154
2009706221145
2010519817145
20111067930454
2012828712266
20139584641,130
20147889615,631
2015649016211
2016829012290
2017781075104
2018104105772
201974107288
202081115682
202183116370
202265137428
202387157826
202462131642
20255817311116
20264511014—

What is it indicated for?

DBSWIN and VistaEasy imaging software are intended for use by qualified dental professionals for windows based diagnostics. The software is a diagnostic aide for licensed radiologists, dentists and clinicians, who perform the actual diagnosis based on their training, qualification, and clinical experience. DBSWIN and VistaEasy are clinical software applications that receive images and data from various imaging sources (i.e., radiography devices and…

Read the full statement (155 words)

DBSWIN and VistaEasy imaging software are intended for use by qualified dental professionals for windows based diagnostics. The software is a diagnostic aide for licensed radiologists, dentists and clinicians, who perform the actual diagnosis based on their training, qualification, and clinical experience. DBSWIN and VistaEasy are clinical software applications that receive images and data from various imaging sources (i.e., radiography devices and digital video capture devices) that are manufactured and distributed by Durr Dental and Air Techniques. It is intended to acquire, display, edit (i.e., resize, adjust contrast, etc.) and distribute images using standard PC hardware. In addition, DBSWIN enables the acquisition of still images from 3rd party TWAIN compliant imaging devices (e.g., generic image devices such as scanners) and the storage and printing of clinical exam data, while VistaEasy distributes the acquired images to 3rd party TWAIN compliant PACS systems for storage and printing.

DBSWIN and VistaEasy software are not intended for mammography use.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K203287: Dbswin, Vistaeasy.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K203287

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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