510(k) Report

510(k) · Cleared

Cleared

Voxelview

K953259510(k) TraditionalCleared Nov 24, 1995135-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

Vital Images, Inc. · LLZ System, Image Processing, Radiological

Cleared on Nov 24, 1995 after a 135-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 36 later devices descend from it.

Decided
Nov 24, 1995
Review
135 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
0

36 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 1996: 1 descendant cleared2006: 1 descendant cleared2008: 2 descendants cleared2024: 1 descendant cleared2023: 3 descendants cleared2016: 4 descendants cleared2012: 2 descendants cleared2009: 1 descendant cleared2010: 1 descendant cleared2011: 1 descendant cleared2015: 1 descendant cleared2013: 2 descendants cleared2017: 5 descendants cleared2018: 3 descendants cleared2022: 1 descendant cleared2014: 1 descendant cleared2025: 3 descendants cleared2019: 1 descendant cleared2021: 2 descendants cleared1995200020052010201520202025
  1. This deviceK953259 VoxelviewVital Images, Inc. · 1995
  2. Descendant · cites it directly · 35 of its ownK963697 Advanced Diagnostic Viewer (Adv)Bio-Vascular, Inc. · 1996
  3. Descendant · 2 generations on · 34 of its ownK063107 3DNET SuiteBiotronics3D, Ltd. · 2006
  4. Descendant · 3 generations on · 31 of its ownK081093 3-D Imaging WorkstationEigen, LLC · 2008
  5. Descendant · 4 generations on · 11 of its ownK153073 UroNav (Version 2.0)Invivo Corporation · 2015
  6. Descendant · 4 generations on · 8 of its ownK093672 Aegis Navigation Anda Egis Pelvic ApplicationSentinelle Medical, Inc. · 2009

Showing 5 of 36 descendants. See all descendants

Descendants cleared per year

1996: 12006: 12008: 22009: 12010: 12011: 12012: 22013: 22014: 12015: 12016: 42017: 52018: 32019: 12021: 22022: 12023: 32024: 12025: 3
1996high 5 (2017) · low 0 (1997)2026

Most influential descendants

Showing 5 of 36 · See all
  • K963697Advanced Diagnostic Viewer (Adv)Bio-Vascular, Inc. · 1996 · cites it directly35descendants
  • K0631073DNET SuiteBiotronics3D, Ltd. · 2006 · 2 generations on34descendants
  • K0810933-D Imaging WorkstationEigen, LLC · 2008 · 3 generations on31descendants
  • K153073UroNav (Version 2.0)Invivo Corporation · 2015 · 4 generations on11descendants
  • K093672Aegis Navigation Anda Egis Pelvic ApplicationSentinelle Medical, Inc. · 2009 · 4 generations on8descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K953259VoxelviewVital Images, Inc.1995—
+1K963697Advanced Diagnostic Viewer (Adv)Bio-Vascular, Inc.1996—
+2K0631073DNET SuiteBiotronics3D, Ltd.2006—
+3K0810933-D Imaging WorkstationEigen, LLC2008—
+4K153073UroNav (Version 2.0)Invivo Corporation2015—
+4K093672Aegis Navigation Anda Egis Pelvic ApplicationSentinelle Medical, Inc.2009—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
200610
200820
200910
201010
201110
201220
201320
201410
201510
201640
201750
201830
201910
202120
202210
202330
202410
202530
FIG. 1 — Lineage of K953259, 1995–2025Source: 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), 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
Get a 510(k) Report

What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (36)

See all 36

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

NumberDeviceApplicantDecidedDescendants
K963697Advanced Diagnostic Viewer (Adv)Bio-Vascular, Inc.199635

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, K963697 (Bio-Vascular, Inc., 1996) has gone furthest, with 35 descendants of its own.

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.

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—

More from Vital Images, Inc.

41 FDA decisions under this applicant name. See the company

  • K181247Vitrea CT Brain PerfusionVital Images, Inc. · 2018
  • K182230Multi Modality ViewerVital Images, Inc. · 2018
  • K172855Vitrea Advanced Visualization, Version 7.6Vital Images, Inc. · 2017
  • K163232Vitrea ViewVital Images, Inc. · 2017
  • K163574Multi Modality ViewerVital Images, Inc. · 2017

Recent decisions in LLZ

The LLZ category page

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  • K261531PV-iCurve ProPerception Vision Medical Technology Co., Ltd. · 2026
  • K263048Syngo Carbon Space (VA4)Siemens Healthineers AG · 2026
  • K261874Syneris PACS v.1.0.1.0Syneris · 2026
  • K262442HipStudio AnalysisReplasia BV · 2026

https://510kreport.com/device/K953259 · printed Nov 4, 2026

Cite this page

510(k) Report. “K953259: Voxelview.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K953259

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026