510(k) Report

510(k) · Cleared

Cleared

CubeVue

K181962510(k) TraditionalCleared Aug 7, 201815-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

Curvebeam, LLC · LLZ System, Image Processing, Radiological

Cleared on Aug 7, 2018 as substantially equivalent to K101342 (Pixmeo Sarl, 2010) after a 15-day review. Its family tree reaches back 8 generations to 1994.

Decided
Aug 7, 2018
Review
15 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K942120 (1994). 11 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 8 generations backK942120 Advantage Windows Diagnostic X-Ray WorkstationGE Medical Systems · 1994
  2. 7 generations backK013630 Isite RadiologyStentor, Inc. · 2001
  3. 6 generations backK031311 Integradweb by Dynamic Imaging, Inc.Dynamic Imaging, Inc. · 2003
  4. 5 generations backK042313 Integradweb MPR/MipDynamic Imaging, Inc. · 2004
  5. 4 generations backK052358 Etiam Star Pacs ComponentsEtiam, S.A. · 2005
  6. 3 generations backK062488 IQ-System Pacs SystemImage Information Systems, Ltd. · 2006
  7. 2 generations backK063470 Aycan Workstation OsirixAycan Digitalsysteme GmbH · 2007
  8. 1 generation backK101342 Osirix MDPixmeo Sarl · 2010
  9. This deviceK181962 CubeVueCurvebeam, LLC · 2018
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K942120Advantage Windows Diagnostic X-Ray WorkstationGE Medical Systems1994—
−7K013630Isite RadiologyStentor, Inc.2001—
−6K031311Integradweb by Dynamic Imaging, Inc.Dynamic Imaging, Inc.2003—
−5K042313Integradweb MPR/MipDynamic Imaging, Inc.2004—
−4K052358Etiam Star Pacs ComponentsEtiam, S.A.2005—
−3K062488IQ-System Pacs SystemImage Information Systems, Ltd.2006—
−2K063470Aycan Workstation OsirixAycan Digitalsysteme GmbH2007—
−1K101342Osirix MDPixmeo Sarl2010—
0 (this device)K181962CubeVueCurvebeam, LLC2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199610
200310
200410
FIG. 1 — Lineage of K181962, 1994–2018Source: 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
*K101342Osirix MD
Summary page 4
…Device name Classification Pixmeo Sarl Osirix MD LLZ K101342 892.2050 Class II This is the first 510(k) submission for this software as a standalone device. Pre…
Pixmeo Sarl2010—

Also cleared against K101342: 8 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 24 years and passes through 8 companies; a new generation was cleared every 1.5 years on median.
  • None of the 11 ancestors has a recall.
  • 8 other devices also cite its predicate K101342.

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. 2018, 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?

CubeVue serves as an accessory to Cone Beam CT extremity imaging devices with the intended use to retrieve, display, and distribute 2D and 3D volumetric image data. The image displaying component allows users to manipulate the images to aid in diagnosis and treatment planning, including rotating and navigating through 3D renderings and 2D MPR slices, adjusting display settings, and making measurements.

It is the User's responsibility to ensure monitor quality and ambient light conditions are consistent with the clinical application.

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. “K181962: CubeVue.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K181962

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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