510(k) · Cleared
Recalled · Class II · 2016Syngo Dynamics, Version 9.0
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Siemens Medical Solutions USA, Inc. · LLZ System, Image Processing, Radiological
Cleared on Oct 5, 2010 as substantially equivalent to K081018 (Siemens Medical Solutions, 2008) after a 68-day review. Its family tree reaches back 7 generations to 1984. 7 later devices descend from it. It has been recalled 7 times.
- Decided
- Oct 5, 2010
- Review
- 68 days
- Class
- Class II
- Product code
- LLZ
- Recalls
- 7
- Predicates
- 1
Its longest line of descent runs back 7 generations to K842308 (1984). 29 ancestors in all. 7 later devices descend from it, 2 citing it directly.
- Root · 7 generations backK842308 12SSL-SCMarquette Electronics, Inc. · 1984
- 6 generations backK980495 Muse Cardiovascular Information SystemMarquette Medical Systems, Inc. · 1998
- 5 generations backK992637 Muse Cardiovascular Information SystemGeneral Electric Medical Systems Information Techn · 1999 · Recalled
- 4 generations backK023100 Accusketch Cardiac Quantitative System W/ Advanced Analysis ComponentsGeneral Electric Medical Systems Information Techn · 2002
- 3 generations backK042525 Centricity Radiology RA600/Centricity Cardiology CA1000/Centricity…Ge Medical Systems Information Technologies · 2004 · Recalled
- 2 generations backK063628 Centricity Radiology RA600, Cardiology CA1000 and Digital HardcopyGe Healthcare Integrated IT Solutions · 2006 · Recalled
- 1 generation backK081018 Syngo Dynamics Version 7.0Siemens Medical Solutions · 2008
- This deviceK102150 Syngo Dynamics, Version 9.0Siemens Medical Solutions USA, Inc. · 2010
- Descendant · cites it directly · 5 of its ownK123922 Syngo DynamicsSiemens Medical Solutions USA, Inc. · 2013
- Descendant · 2 generations on · 4 of its ownK171053 syngo Dynamics Version VA30Siemens Healthcare GmbH · 2017
- Descendant · 3 generations on · 3 of its ownK220832 syngo Dynamics (Version VA40E)Siemens Medical Solutions USA, Inc. · 2022
- Descendant · 4 generations on · 2 of its ownK222428 Syngo Dynamics (Version VA40F)Siemens Medical Solutions USA, Inc. · 2022
- Descendant · 5 generations on · 1 of its ownK242551 syngo Dynamics (Version VA41D)Siemens Healthcare GmbH · 2025
Showing 5 of 7 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 7 · See all- K123922Syngo DynamicsSiemens Medical Solutions USA, Inc. · 2013 · cites it directly5descendants
- K171053syngo Dynamics Version VA30Siemens Healthcare GmbH · 2017 · 2 generations on4descendants
- K220832syngo Dynamics (Version VA40E)Siemens Medical Solutions USA, Inc. · 2022 · 3 generations on3descendants
- K222428Syngo Dynamics (Version VA40F)Siemens Medical Solutions USA, Inc. · 2022 · 4 generations on2descendants
- K242551syngo Dynamics (Version VA41D)Siemens Healthcare GmbH · 2025 · 5 generations on1descendant
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −7 | K842308 | 12SSL-SC | Marquette Electronics, Inc. | 1984 | — |
| −6 | K980495 | Muse Cardiovascular Information System | Marquette Medical Systems, Inc. | 1998 | — |
| −5 | K992637 | Muse Cardiovascular Information System | General Electric Medical Systems Information Techn | 1999 | 1 |
| −4 | K023100 | Accusketch Cardiac Quantitative System W/ Advanced Analysis Components | General Electric Medical Systems Information Techn | 2002 | — |
| −3 | K042525 | Centricity Radiology RA600/Centricity Cardiology CA1000/Centricity Digital… | Ge Medical Systems Information Technologies | 2004 | 3 |
| −2 | K063628 | Centricity Radiology RA600, Cardiology CA1000 and Digital Hardcopy | Ge Healthcare Integrated IT Solutions | 2006 | 3 |
| −1 | K081018 | Syngo Dynamics Version 7.0 | Siemens Medical Solutions | 2008 | — |
| 0 (this device) | K102150 | Syngo Dynamics, Version 9.0 | Siemens Medical Solutions USA, Inc. | 2010 | — |
| +1 | K123922 | Syngo Dynamics | Siemens Medical Solutions USA, Inc. | 2013 | — |
| +2 | K171053 | syngo Dynamics Version VA30 | Siemens Healthcare GmbH | 2017 | — |
| +3 | K220832 | syngo Dynamics (Version VA40E) | Siemens Medical Solutions USA, Inc. | 2022 | — |
| +4 | K222428 | Syngo Dynamics (Version VA40F) | Siemens Medical Solutions USA, Inc. | 2022 | — |
| +5 | K242551 | syngo Dynamics (Version VA41D) | Siemens Healthcare GmbH | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1984 | 1 | 0 |
| 1989 | 1 | 0 |
| 1990 | 1 | 0 |
| 1991 | 2 | 0 |
| 1993 | 1 | 0 |
| 1995 | 2 | 0 |
| 1996 | 3 | 0 |
| 1997 | 1 | 0 |
| 1998 | 1 | 0 |
| 2000 | 2 | 0 |
| 2001 | 1 | 0 |
| 2002 | 2 | 0 |
| 2004 | 2 | 0 |
| 2006 | 1 | 0 |
| 2007 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2012 | 1 | 0 |
| 2013 | 1 | 0 |
| 2017 | 1 | 0 |
| 2022 | 2 | 0 |
| 2025 | 1 | 0 |
| 2026 | 1 | 0 |
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 K230955 syngo Application Softwarescore 21.5 · 11 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K081018 | Syngo Dynamics Version 7.0 | 2008 |
What descends from it? (7)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Jan 29, 2016 | Class II | Z-0826-2016 | Software design | Siemens is releasing a software update that addresses an issue of mixing data from multiple patients. In rare situations, echo trend graphs may mix data from multiple patients. |
| Jan 25, 2016 | Class II | Z-1183-2016 | Software design | Siemens' conducting a recall due to a potential issue when using the measurement package of the VA10 version of syngo Dynamics. |
| Apr 3, 2014 | Class II | Z-1613-2014 | Software design | Systems with the affected serial number are experiencing a software error which may lead to incorrect patient demographics display. |
| Jan 27, 2014 | Class II | Z-1216-2014 | Software design | Potential patient data mixup. Improper error handling could allow for two different patients to be displayed in syngo Dynamics. Images shown for one patient and reporting system shown for a different patient, leading to the potential for… |
| Jun 10, 2013 | Class II | Z-1859-2013 | Software design | Siemens initiate this recall due to a potential issue when using the sDIS matching rules of the syngo Dynamics Information System version 9.5 or VA10A with modality device configured to end study at association close. Images or DICOM SR… |
| Jul 13, 2012 | Class II | Z-2219-2012 | Software design | If multiple uncompressed images/clips are sent to the syngo Dynamics server, around the same time, it is possible for an image from a patient to be placed in another patient's study. |
| Mar 24, 2011 | Not classified | Z-2293-2011 | Software design | If one or more graphs are in a table on the report, and if any of those graphs are deleted, it may lead to reports failing to save and/or marking the study as read might leave the study in an unread state or might mark the study as read… |
The 5 latest of 7 recalls; the web page lists all.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 26 years and passes through 7 companies; a new generation was cleared every 2.2 years on median.
- 10 of the 29 ancestors have a recall of any class.
- Of its descendants, K123922 (Siemens Medical Solutions USA, Inc., 2013) has gone furthest, with 5 descendants of its own.
How does its category compare?
All LLZ devicesLLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.
FDA decisions per year · LLZ
58in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LLZ
173in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LLZ
11in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LLZ
116in 2025
MAUDE reports naming product code LLZ, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 76 | 36 | 20 | 152 |
| 2008 | 94 | 52 | 32 | 154 |
| 2009 | 70 | 62 | 21 | 145 |
| 2010 | 51 | 98 | 17 | 145 |
| 2011 | 106 | 79 | 30 | 454 |
| 2012 | 82 | 87 | 12 | 266 |
| 2013 | 95 | 84 | 64 | 1,130 |
| 2014 | 78 | 89 | 6 | 15,631 |
| 2015 | 64 | 90 | 16 | 211 |
| 2016 | 82 | 90 | 12 | 290 |
| 2017 | 78 | 107 | 5 | 104 |
| 2018 | 104 | 105 | 7 | 72 |
| 2019 | 74 | 107 | 2 | 88 |
| 2020 | 81 | 115 | 6 | 82 |
| 2021 | 83 | 116 | 3 | 70 |
| 2022 | 65 | 137 | 4 | 28 |
| 2023 | 87 | 157 | 8 | 26 |
| 2024 | 62 | 131 | 6 | 42 |
| 2025 | 58 | 173 | 11 | 116 |
| 2026 | 45 | 110 | 14 | — |
What is it indicated for?
syngo® Dynamics is a Picture Archiving and Communication System (PACS) Intended for acceptance, transfer, display, storage, archive and manipulation of digital medical images, including quantification and report generation.
syngo® Dynamics is not intended to be used for reading of mammography images.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K102150 · printed Nov 6, 2026
Cite this page
510(k) Report. “K102150: Syngo Dynamics, Version 9.0.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K102150
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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