510(k) Report

510(k) · Cleared

Cleared

JiveX

K142750510(k) TraditionalCleared Jun 26, 2015275-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

Visus Technology Transfer GmbH · LLZ System, Image Processing, Radiological

Cleared on Jun 26, 2015 as substantially equivalent to K053183 (Visus Technology Transfer GmbH, 2006) and 1 other predicate after a 275-day review. Its family tree reaches back 9 generations to 1997. 6 later devices descend from it.

Decided
Jun 26, 2015
Review
275 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
2

Its longest line of descent runs back 9 generations to K971684 (1997). 27 ancestors in all, the oldest K945188 (1995). 6 later devices descend from it, 2 citing it directly.

Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor3 generations back: 2 other ancestors4 generations back: 2 other ancestors5 generations back: 1 other ancestor6 generations back: 2 other ancestors7 generations back: 8 other ancestors8 generations back: 1 other ancestor9 generations back: 1 other ancestor 1 generation forward: 2 descendants2 generations forward: 1 descendant3 generations forward: 1 descendant4 generations forward: 1 descendant5 generations forward: 1 descendant K132532 · Syngo.Plaza VB10A · Siemens AG Healthcare · 2013 · recalledK101666 · Syngo. Plaza VA20A · Siemens AG Medical Solutions · 2010 · recalledK092519 · Syngo.X · Siemens AG Medical Solutions · 2009 · recalledK072728 · Syngo Multimodality Workplace · Siemens AG Medical Solutions · 2008K061964 · Syngo Multimodality Workplace · Siemens AG Medical Solutions · 2006K052423 · Magnetom Systems with Syngo Expert - I Option · Siemens Medi Cal Solutions, Inc. · 2006K041112 · Magnetom Espree System · Siemens Medical Solutions USA, Inc. · 2004 · recalledK032428 · Magnetom Avanto MR System · Siemens Medical Solutions USA, Inc. · 2003 · recalledK971684 · Magnetom Project 047 System (Numaris 3.5 Software) · Siemens Medical Solutions USA, Inc. · 1997 · recalled−50+5
  1. Root · 9 generations backK971684 Magnetom Project 047 System (Numaris 3.5 Software)Siemens Medical Solutions USA, Inc. · 1997 · Recalled
  2. 5 generations between
  3. 3 generations backK092519 Syngo.XSiemens AG Medical Solutions · 2009 · Recalled
  4. 2 generations backK101666 Syngo. Plaza VA20ASiemens AG Medical Solutions · 2010 · Recalled
  5. 1 generation backK132532 Syngo.Plaza VB10ASiemens AG Healthcare · 2013 · Recalled
  6. This deviceK142750 JiveXVisus Technology Transfer GmbH · 2015
  7. Descendant · cites it directly · 4 of its ownK162008 JiveXVisus Technology Transfer GmbH · 2016
  8. Descendant · 2 generations on · 3 of its ownK181964 JiveXVisus Health IT GmbH · 2018
  9. Descendant · 3 generations on · 2 of its ownK200703 JiveXVisus Health IT GmbH · 2020
  10. Descendant · 4 generations on · 1 of its ownK212321 JiveX (Model Number / Release: 5.3)Visus Health IT GmbH · 2021
  11. Descendant · 5 generations on · 0 of its ownK231041 JiveX (Model Number / Release: 5.4)Visus Health IT GmbH · 2023
Show all 9 generations
  1. Root · 9 generations backK971684 Magnetom Project 047 System (Numaris 3.5 Software)Siemens Medical Solutions USA, Inc. · 1997 · Recalled
  2. 8 generations backK032428 Magnetom Avanto MR SystemSiemens Medical Solutions USA, Inc. · 2003 · Recalled
  3. 7 generations backK041112 Magnetom Espree SystemSiemens Medical Solutions USA, Inc. · 2004 · Recalled
  4. 6 generations backK052423 Magnetom Systems with Syngo Expert - I OptionSiemens Medi Cal Solutions, Inc. · 2006
  5. 5 generations backK061964 Syngo Multimodality WorkplaceSiemens AG Medical Solutions · 2006
  6. 4 generations backK072728 Syngo Multimodality WorkplaceSiemens AG Medical Solutions · 2008
  7. 3 generations backK092519 Syngo.XSiemens AG Medical Solutions · 2009 · Recalled
  8. 2 generations backK101666 Syngo. Plaza VA20ASiemens AG Medical Solutions · 2010 · Recalled
  9. 1 generation backK132532 Syngo.Plaza VB10ASiemens AG Healthcare · 2013 · Recalled
  10. This deviceK142750 JiveXVisus Technology Transfer GmbH · 2015

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2016: 12018: 12020: 22021: 12023: 1
2016high 2 (2020) · low 0 (2017)2026

Most influential descendants

Showing 5 of 6 · See all
  • K162008JiveXVisus Technology Transfer GmbH · 2016 · cites it directly4descendants
  • K181964JiveXVisus Health IT GmbH · 2018 · 2 generations on3descendants
  • K200703JiveXVisus Health IT GmbH · 2020 · 3 generations on2descendants
  • K212321JiveX (Model Number / Release: 5.3)Visus Health IT GmbH · 2021 · 4 generations on1descendant
  • K231041JiveX (Model Number / Release: 5.4)Visus Health IT GmbH · 2023 · 5 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K971684Magnetom Project 047 System (Numaris 3.5 Software)Siemens Medical Solutions USA, Inc.19974
−8K032428Magnetom Avanto MR SystemSiemens Medical Solutions USA, Inc.20034
−7K041112Magnetom Espree SystemSiemens Medical Solutions USA, Inc.20044
−6K052423Magnetom Systems with Syngo Expert - I OptionSiemens Medi Cal Solutions, Inc.2006—
−5K061964Syngo Multimodality WorkplaceSiemens AG Medical Solutions2006—
−4K072728Syngo Multimodality WorkplaceSiemens AG Medical Solutions2008—
−3K092519Syngo.XSiemens AG Medical Solutions20094
−2K101666Syngo. Plaza VA20ASiemens AG Medical Solutions20103
−1K132532Syngo.Plaza VB10ASiemens AG Healthcare201311
0 (this device)K142750JiveXVisus Technology Transfer GmbH2015—
+1K162008JiveXVisus Technology Transfer GmbH2016—
+2K181964JiveXVisus Health IT GmbH2018—
+3K200703JiveXVisus Health IT GmbH2020—
+4K212321JiveX (Model Number / Release: 5.3)Visus Health IT GmbH2021—
+5K231041JiveX (Model Number / Release: 5.4)Visus Health IT GmbH2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
199610
199720
199910
200020
200120
200530
200610
200720
200820
201010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
201810
202020
202110
202310
FIG. 1 — Lineage of K142750, 1997–2023Source: 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
Get a 510(k) Report

What was it cleared against? (2)

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
*K053183Jive X Software
Summary page 5
…h the predicate devices syngo.plaza and JiveX SE: syngo.plaza SE: JiveX JiveX 510(k) number K132532 K053183 SIEMENS AG, VISUS Technology VISUS Technology Medical Solutions…
Visus Technology Transfer GmbH2006—
*K132532Syngo.Plaza VB10A
Summary page 5
…table compares JiveX with the predicate devices syngo.plaza and JiveX SE: syngo.plaza SE: JiveX JiveX 510(k) number K132532 K053183 SIEMENS AG, VISUS Technology VISUS Technology…
Siemens AG Healthcare201311

What descends from it? (6)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K162008JiveXVisus Technology Transfer GmbH20164
K200132AshvinsMedicalcommunications GmbH20200

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 18 years and passes through 5 companies; a new generation was cleared every 1.5 years on median.
  • 15 of the 27 ancestors have a recall of any class.
  • Of its descendants, K162008 (Visus Technology Transfer GmbH, 2016) has gone furthest, with 4 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. 2015, 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?

JiveX is a software only Picture Archiving and Communication System intended to display, process, read, report, communicate, distribute, store, and archive medical data which is available as DICOM or HL7 data, including mammographic images, and bio signals. JiveX also converts case related non-image documents, archives them as DICOM data and serves as a vendor neutral archive. It supports the physician in diagnosis. For primary image diagnosis in…

Read the full statement (125 words)

JiveX is a software only Picture Archiving and Communication System intended to display, process, read, report, communicate, distribute, store, and archive medical data which is available as DICOM or HL7 data, including mammographic images, and bio signals. JiveX also converts case related non-image documents, archives them as DICOM data and serves as a vendor neutral archive.

It supports the physician in diagnosis.

For primary image diagnosis in Mammography only uncompressed or non-lossy compressed images must be used. Also monitors (displays) and printers which received FDA clearance for Mammography must be used.

Typical users of this system are trained professionals, including but not limited to physicians, radiologists, nurses, medical technicians, and assistants.

Note: Web-based image distribution and mobile device display are not intended for diagnostic purposes.

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. “K142750: JiveX.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K142750

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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