510(k) Report

510(k) · Cleared

Cleared

Synapse 3D Lung and Abdomen Analysis

K120648510(k) TraditionalCleared Jun 14, 2012104-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

Fujifilm Medical System U.S.A., Inc. · LLZ System, Image Processing, Radiological

Cleared on Jun 14, 2012 as substantially equivalent to K083227 (Vida Diagnostics, Inc., 2008) after a 104-day review. Its family tree reaches back 7 generations to 1995. 10 later devices descend from it.

Decided
Jun 14, 2012
Review
104 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K954355 (1995). 11 ancestors in all. 10 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1996: 1 other ancestor2000: 1 other ancestor1998: 2 other ancestors2013: 1 descendant cleared2015: 1 descendant cleared2023: 1 descendant cleared2018: 1 descendant cleared2021: 1 descendant cleared2020: 1 descendant cleared2026: 2 descendants cleared2024: 1 descendant cleared2025: 1 descendant clearedK954355 · Advantage Windows 3D with Navigator Option · General Electric Co. · 1995K974715 · Advantage 3D XR · GE Medical Systems · 1998K984634 · 3D-Angio · Siemens Medical Corp. · 1999K011447 · IN Space 3D · Siemens Medical Solutions USA, Inc. · 2001K043469 · Syngo Inspace 4D · Siemens AG Medical Solutions · 2005K071513 · Inspace 4D Software Package with Extended Functionality · Siemens Medical Solutions · 2007K083227 · Vida Pulmonary Workstation 2 (PW2) · Vida Diagnostics, Inc. · 20081995200020052010201520202025
Other ancestors, by generationDescendants, by generation 3 generations back: 1 other ancestor5 generations back: 2 other ancestors6 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 3 descendants3 generations forward: 3 descendants4 generations forward: 2 descendants5 generations forward: 1 descendant K083227 · Vida Pulmonary Workstation 2 (PW2) · Vida Diagnostics, Inc. · 2008K071513 · Inspace 4D Software Package with Extended Functionality · Siemens Medical Solutions · 2007K043469 · Syngo Inspace 4D · Siemens AG Medical Solutions · 2005K011447 · IN Space 3D · Siemens Medical Solutions USA, Inc. · 2001K984634 · 3D-Angio · Siemens Medical Corp. · 1999K974715 · Advantage 3D XR · GE Medical Systems · 1998K954355 · Advantage Windows 3D with Navigator Option · General Electric Co. · 1995−50+5
  1. Root · 7 generations backK954355 Advantage Windows 3D with Navigator OptionGeneral Electric Co. · 1995
  2. 6 generations backK974715 Advantage 3D XRGE Medical Systems · 1998
  3. 5 generations backK984634 3D-AngioSiemens Medical Corp. · 1999
  4. 4 generations backK011447 IN Space 3DSiemens Medical Solutions USA, Inc. · 2001
  5. 3 generations backK043469 Syngo Inspace 4DSiemens AG Medical Solutions · 2005
  6. 2 generations backK071513 Inspace 4D Software Package with Extended FunctionalitySiemens Medical Solutions · 2007
  7. 1 generation backK083227 Vida Pulmonary Workstation 2 (PW2)Vida Diagnostics, Inc. · 2008
  8. This deviceK120648 Synapse 3D Lung and Abdomen AnalysisFujifilm Medical System U.S.A., Inc. · 2012
  9. Descendant · cites it directly · 9 of its ownK130542 Synapse 3D Lung and Abdomen AnalysisFujifilm Medical System U.S.A., Inc. · 2013
  10. Descendant · 2 generations on · 4 of its ownK151988 Visible Patient SuiteVisible Patient, Sas · 2015
  11. Descendant · 3 generations on · 3 of its ownK212896 Visible Patient SuiteVisible Patient, Sas · 2021
  12. Descendant · 4 generations on · 1 of its ownK250237 InferOperate SuiteBeijing Infervision Healthcare Medical Technology Co., Ltd. · 2025
  13. Descendant · 2 generations on · 1 of its ownK223556 DeepCatchMedical IP Co., Ltd. · 2023

Showing 5 of 10 descendants. See all descendants

Descendants cleared per year

2013: 12015: 12018: 12020: 12021: 12023: 12024: 12025: 12026: 2
2013high 2 (2026) · low 0 (2014)2026

Most influential descendants

Showing 5 of 10 · See all
  • K130542Synapse 3D Lung and Abdomen AnalysisFujifilm Medical System U.S.A., Inc. · 2013 · cites it directly9descendants
  • K151988Visible Patient SuiteVisible Patient, Sas · 2015 · 2 generations on4descendants
  • K212896Visible Patient SuiteVisible Patient, Sas · 2021 · 3 generations on3descendants
  • K250237InferOperate SuiteBeijing Infervision Healthcare Medical Technology Co., Ltd. · 2025 · 4 generations on1descendant
  • K223556DeepCatchMedical IP Co., Ltd. · 2023 · 2 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K954355Advantage Windows 3D with Navigator OptionGeneral Electric Co.1995—
−6K974715Advantage 3D XRGE Medical Systems1998—
−5K9846343D-AngioSiemens Medical Corp.1999—
−4K011447IN Space 3DSiemens Medical Solutions USA, Inc.2001—
−3K043469Syngo Inspace 4DSiemens AG Medical Solutions2005—
−2K071513Inspace 4D Software Package with Extended FunctionalitySiemens Medical Solutions2007—
−1K083227Vida Pulmonary Workstation 2 (PW2)Vida Diagnostics, Inc.2008—
0 (this device)K120648Synapse 3D Lung and Abdomen AnalysisFujifilm Medical System U.S.A., Inc.2012—
+1K130542Synapse 3D Lung and Abdomen AnalysisFujifilm Medical System U.S.A., Inc.2013—
+2K151988Visible Patient SuiteVisible Patient, Sas2015—
+3K212896Visible Patient SuiteVisible Patient, Sas2021—
+4K250237InferOperate SuiteBeijing Infervision Healthcare Medical Technology Co., Ltd.2025—
+2K223556DeepCatchMedical IP Co., Ltd.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199610
199820
200010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201310
201510
201810
202010
202110
202310
202410
202510
202620
FIG. 1 — Lineage of K120648, 1995–2026Source: 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; numbers the summary cites that cannot be its predicate are marked – and kept off the family tree.

TypeNumberDeviceApplicantDecidedRecalls
Kept off the family treeK1103720Synapse 3D Lung and Abdomen Analysis
Number could not be read
*K083227Vida Pulmonary Workstation 2 (PW2)
Summary page 2
…Abdomen Analysis (V3.0) 510O(k) Predicate Device: * Synapse 3D Lung and Abdomen Analysis (K1I03720), FUJIFILM Medical Systems U.S.A., Inc. " Pulmonary Workstation 2 (K083227), VIDA Diagnostics, Inc. Descriptbon of the Device Synapse 3D Lung and Abdomen Analysis (V3.0) is the updated version of previou…
Vida Diagnostics, Inc.2008—

Also cleared against K083227: 11 other devices →

What descends from it? (10)

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

NumberDeviceApplicantDecidedDescendants
K130542Synapse 3D Lung and Abdomen AnalysisFujifilm Medical System U.S.A., Inc.20139

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 17 years and passes through 8 companies; a new generation was cleared every 2.4 years on median.
  • 1 of the 11 ancestors has a recall of any class.
  • Of its descendants, K130542 (Fujifilm Medical System U.S.A., Inc., 2013) has gone furthest, with 9 descendants of its own.
  • 11 other devices also cite its predicate K083227.

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. 2012, 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?

Synapse 3D Lung and Abdomen Analysis is medical imaging software used with Synapse 3D Base Tools that is intended to provide trained medical professionals With tools to aid them in reading, interpreting, reporting, and treatment planning. Synapse 3D Lung and Abdomen Analysis accepts DICOM compliant medical images acquired from CT. This product is not intended for use with or for the primary diagnostic interpretation of Mammography images. Addition to…

Read the full statement (172 words)

Synapse 3D Lung and Abdomen Analysis is medical imaging software used with Synapse 3D Base Tools that is intended to provide trained medical professionals With tools to aid them in reading, interpreting, reporting, and treatment planning. Synapse 3D Lung and Abdomen Analysis accepts DICOM compliant medical images acquired from CT.

This product is not intended for use with or for the primary diagnostic interpretation of Mammography images.

Addition to Synapse 3D Base Tools, Synapse 3D Lung and Abdomen Analysis isintended to;

> use non-contrast and contrast enhanced computed tornographic images of the lung, provide custom vvrkflowvs and UI, and reporting functions for lung analysis including boundary detection and volume calculation for pulmonary nodules in the lung based on the location specified by the user-, segmentation of bronchial tubes in the lung, approximation of air supply region by the user specified bronchial tube, identifying, displaying and processing low absorption regions in the lung.

> use non-contrasted CT images and calculate subaitaneous fat and visceral fat areas in 2D and both volumes i 3D.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K120648: Synapse 3D Lung and Abdomen Analysis.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K120648

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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