510(k) · Cleared
ClearedUC-CARE NaviGo Workstation
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
UC-CARE, Ltd. · LLZ System, Image Processing, Radiological
Cleared on Feb 6, 2017 as substantially equivalent to K100784 (UC-CARE, Ltd., 2011) and 1 other predicate after a 308-day review. Its family tree reaches back 7 generations to 1996. 2 later devices descend from it.
- Decided
- Feb 6, 2017
- Review
- 308 days
- Class
- Class II
- Product code
- LLZ
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 7 generations to K954678 (1996). 13 ancestors in all, the oldest K953259 (1995). 2 later devices descend from it, 1 citing it directly.
- Root · 7 generations backK954678 Pro VisionAlgotec Systems, Ltd. · 1996
- 6 generations backK980648 Pro VisionAlgotec Systems, Ltd. · 1998
- 5 generations backK992654 Plug 'N View 3D, Version 1.0Voxar Limited · 1999
- 4 generations backK063107 3DNET SuiteBiotronics3D, Ltd. · 2006
- 3 generations backK081093 3-D Imaging WorkstationEigen, LLC · 2008
- 2 generations backK100793 Urostation 3D Prostate SuiteKoelis · 2010
- 1 generation backK131448 3D Prostate Suite 3DTRUS Prostate Mapping, Mri/3DTRUS Fusion Option…Koelis · 2013
- This deviceK160934 UC-CARE NaviGo WorkstationUC-CARE, Ltd. · 2017
- Descendant · cites it directly · 1 of its ownK173054 Navigo Workstation Version 2.0UC-CARE, Ltd. · 2018
- Descendant · 2 generations on · 0 of its ownK250664 Navigo Workstation 2.3 (FPRMC00039)UC-CARE, Ltd. · 2025
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −7 | K954678 | Pro Vision | Algotec Systems, Ltd. | 1996 | — |
| −6 | K980648 | Pro Vision | Algotec Systems, Ltd. | 1998 | — |
| −5 | K992654 | Plug 'N View 3D, Version 1.0 | Voxar Limited | 1999 | — |
| −4 | K063107 | 3DNET Suite | Biotronics3D, Ltd. | 2006 | — |
| −3 | K081093 | 3-D Imaging Workstation | Eigen, LLC | 2008 | — |
| −2 | K100793 | Urostation 3D Prostate Suite | Koelis | 2010 | — |
| −1 | K131448 | 3D Prostate Suite 3DTRUS Prostate Mapping, Mri/3DTRUS Fusion Option, Second… | Koelis | 2013 | — |
| 0 (this device) | K160934 | UC-CARE NaviGo Workstation | UC-CARE, Ltd. | 2017 | — |
| +1 | K173054 | Navigo Workstation Version 2.0 | UC-CARE, Ltd. | 2018 | — |
| +2 | K250664 | Navigo Workstation 2.3 (FPRMC00039) | UC-CARE, Ltd. | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1995 | 1 | 0 |
| 1996 | 1 | 0 |
| 2000 | 1 | 0 |
| 2003 | 1 | 0 |
| 2005 | 1 | 0 |
| 2011 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2018 | 1 | 0 |
| 2025 | 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? (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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K100784 | UC-Care Navigo SytemSummary page 4…ces, product code: LLZ, Regulation Number: 892.2050, reviewed by the Division of Radiology. Predicate Devices: Primary: NaviGo™ Workstation (UC-CARE Ltd.), cleared under K100784, concurrence date November 1, 2011. Secondary: Urostation – 3D Prostate Suite (Koelis), cleared under K131448, concurrence date J… | 2011 |
| * | K131448 | 3D Prostate Suite 3DTRUS Prostate Mapping, Mri/3DTRUS Fusion Option, Second Look 3DTRUS…Summary page 4…Primary: NaviGo™ Workstation (UC-CARE Ltd.), cleared under K100784, concurrence date November 1, 2011. Secondary: Urostation – 3D Prostate Suite (Koelis), cleared under K131448, concurrence date July 26, 2013. UC-CARE Ltd. PO Box 67, Yokneam 20692, Isra… | 2013 |
What descends from it? (2)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K173054 | Navigo Workstation Version 2.0 | 2018 | 1 |
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 21 years and passes through 6 companies; a new generation was cleared every 2.5 years on median.
- 2 of the 13 ancestors have a recall of any class.
- Of its descendants, K173054 (UC-CARE, Ltd., 2018) has gone furthest, with 1 descendant 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. 2017, 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?
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) with the ultrasound images and thus superimpose information from one modality onto the other. Additional software features include patient…
Read the full statement (138 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) with the ultrasound images and thus superimpose information from one modality onto the other. Additional software features include patient data management, multi-planar reconstruction, segmentation, image measurement and 3-D image registration.
The device is specifically indicated to provide information on regional orientation within the prostate to assist needle targeted procedures (e.g. biopsy) regions of interest display, procedures planning and, reconstruction of a 3D rendered surface model of the prostate display needle locations that have been selected by the physician, as well as storage and future retrieval of this information.
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/K160934 · printed Nov 4, 2026
Cite this page
510(k) Report. “K160934: UC-CARE NaviGo Workstation.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K160934
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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