510(k) Report

510(k) · Cleared

Cleared

Navigo Workstation Version 2.0

K173054510(k) TraditionalCleared Jan 16, 2018110-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

UC-CARE, Ltd. · LLZ System, Image Processing, Radiological

Cleared on Jan 16, 2018 as substantially equivalent to K160934 (UC-CARE, Ltd., 2017) and 1 other predicate after a 110-day review. Its family tree reaches back 8 generations to 1996. 1 later device descends from it.

Decided
Jan 16, 2018
Review
110 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K954678 (1996). 15 ancestors in all, the oldest K953259 (1995). 1 later device descends from it, 1 citing it directly.

  1. Root · 8 generations backK954678 Pro VisionAlgotec Systems, Ltd. · 1996
  2. 7 generations backK980648 Pro VisionAlgotec Systems, Ltd. · 1998
  3. 6 generations backK992654 Plug 'N View 3D, Version 1.0Voxar Limited · 1999
  4. 5 generations backK063107 3DNET SuiteBiotronics3D, Ltd. · 2006
  5. 4 generations backK081093 3-D Imaging WorkstationEigen, LLC · 2008
  6. 3 generations backK100793 Urostation 3D Prostate SuiteKoelis · 2010
  7. 2 generations backK131448 3D Prostate Suite 3DTRUS Prostate Mapping, Mri/3DTRUS Fusion Option…Koelis · 2013
  8. 1 generation backK160934 UC-CARE NaviGo WorkstationUC-CARE, Ltd. · 2017
  9. This deviceK173054 Navigo Workstation Version 2.0UC-CARE, Ltd. · 2018
  10. Descendant · cites it directly · 0 of its ownK250664 Navigo Workstation 2.3 (FPRMC00039)UC-CARE, Ltd. · 2025

Most influential descendants

Showing 1 of 1 · See all
  • K250664Navigo Workstation 2.3 (FPRMC00039)UC-CARE, Ltd. · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K954678Pro VisionAlgotec Systems, Ltd.1996—
−7K980648Pro VisionAlgotec Systems, Ltd.1998—
−6K992654Plug 'N View 3D, Version 1.0Voxar Limited1999—
−5K0631073DNET SuiteBiotronics3D, Ltd.2006—
−4K0810933-D Imaging WorkstationEigen, LLC2008—
−3K100793Urostation 3D Prostate SuiteKoelis2010—
−2K1314483D Prostate Suite 3DTRUS Prostate Mapping, Mri/3DTRUS Fusion Option, Second…Koelis2013—
−1K160934UC-CARE NaviGo WorkstationUC-CARE, Ltd.2017—
0 (this device)K173054Navigo Workstation Version 2.0UC-CARE, Ltd.2018—
+1K250664Navigo Workstation 2.3 (FPRMC00039)UC-CARE, Ltd.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
199610
200010
200310
200510
201110
201510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
FIG. 1 — Lineage of K173054, 1996–2025Source: 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), 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
*K160934UC-CARE NaviGo Workstation
Summary page 4
…ving and communications system Regulatory Class: II Regulation Number: 21 CFR 892.2050 Product Code: LLZ Predicate Devices UC-Care Ltd.’s Navigo Workstation K160934 InVivo Corporation's Uronav (Version 2.0) K153073 Device Description The Navigo Workstation Version 2.0 is an ad…
UC-CARE, Ltd.2017—
*K153073UroNav (Version 2.0)
Summary page 4
…lation Number: 21 CFR 892.2050 Product Code: LLZ Predicate Devices UC-Care Ltd.’s Navigo Workstation K160934 InVivo Corporation's Uronav (Version 2.0) K153073 Device Description The Navigo Workstation Version 2.0 is an adjunctive tool in the management of prostate diagnos…
Invivo Corporation2015—

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K250664Navigo Workstation 2.3 (FPRMC00039)UC-CARE, Ltd.20250

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 22 years and passes through 6 companies; a new generation was cleared every 2.5 years on median.
  • 2 of the 15 ancestors have a recall of any class.
  • Of its descendants, K250664 (UC-CARE, Ltd., 2025) has gone furthest, with 0 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. 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?

The UC-Care Navigo Workstation is an adjunctive tool for ultrasound guided procedures and is intended to be used by physicians in the clinic or hospital for 2-D and 3-D visualization of ultrasound images of the prostate gland. The Navigo Workstation offers the ability to fuse DICOM originated information (e.g. MRI, CT) with the ultrasound images and thus superimposes information from one modality onto the other. It also provides the ability to display a…

Read the full statement (203 words)

The UC-Care Navigo Workstation is an adjunctive tool for ultrasound guided procedures and is intended to be used by physicians in the clinic or hospital for 2-D and 3-D visualization of ultrasound images of the prostate gland. The Navigo Workstation offers the ability to fuse DICOM originated information (e.g. MRI, CT) with the ultrasound images and thus superimposes information from one modality onto the other.

It also provides the ability to display a simulated image of a tracked insertion tool such as a needle, guide wire, catheter, grid plate or probe on a computer monitor screen that shows images of the target organ and the current and the projected future path of the interventional instrument taking into account patient movement. Additional software features include patient data management, multiplanar reconstruction, segmentation, image measurement and 3-D image registration, as well as storage and future retrieval of this information.

Navigo is intended for treatment planning and guidance for clinical, interventional and/or diagnostic procedures. The device is intended to be used in interventional and diagnostic procedures in a clinical setting. Example procedures include, but are not limited to image fusion for diagnostic clinical examinations and procedures, soft tissue biopsies, soft tissue ablations and placement of fiducial markers.

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. “K173054: Navigo Workstation Version 2.0.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K173054

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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