510(k) · Cleared
Recalled · Class II · 2024UNiD Spine Analyzer
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medicrea International, Inc. · LLZ System, Image Processing, Radiological
Cleared on Jan 12, 2022 as substantially equivalent to K180091 (Medicrea International, 2018) after a 198-day review. Its family tree reaches back 12 generations to 1990. 2 later devices descend from it. It has been recalled once.
- Decided
- Jan 12, 2022
- Review
- 198 days
- Class
- Class II
- Product code
- LLZ
- Recalls
- 1
- Predicates
- 1
Its longest line of descent runs back 12 generations to K896095 (1990). 25 ancestors in all. 2 later devices descend from it, 1 citing it directly.
- Root · 12 generations backK896095 Images-on-Call Teleradiology SystemDevices & Services Co. · 1990
- 8 generations between
- 3 generations backK141669 SurgimapNemaris, Inc. · 2014
- 2 generations backK170172 UNiD Spine AnalyzerMedicrea International · 2017
- 1 generation backK180091 UNiD Spine AnalyzerMedicrea International · 2018
- This deviceK212005 UNiD Spine AnalyzerMedicrea International, Inc. · 2022
- Descendant · cites it directly · 1 of its ownK251629 UNiD™ Spine AnalyzerMedicrea International S.A.S. (Medtronic) · 2025
- Descendant · 2 generations on · 0 of its ownK261289 UNiD™ Spine Analyzer (SW3002)Medicrea International S.A.S. (Medtronic) · 2026
Show all 12 generations
- Root · 12 generations backK896095 Images-on-Call Teleradiology SystemDevices & Services Co. · 1990
- 11 generations backK962699 Radworks Medical Imaging SoftwareApplicare Medical Imaging, B.V. · 1996
- 10 generations backK982862 Radworks Medical Imaging Software with Quality Control ModuleApplicare Medical Imaging, B.V. · 1998
- 9 generations backK012211 Efilm WorkstationEfilm Medical, Inc. · 2001 · Recalled
- 8 generations backK020995 Efilm Workstation with ModulesEfilm Medical, Inc. · 2002 · Recalled
- 7 generations backK032401 OrthoviewOmsbar, Ltd. · 2003
- 6 generations backK042816 Traumacad 1.2Orthocrat, Ltd. · 2004
- 5 generations backK073714 Traumacad Version 2.0Orthocrat, Ltd. · 2008
- 4 generations backK111019 Surgimap (TM) SpineNemaris, Inc. · 2011
- 3 generations backK141669 SurgimapNemaris, Inc. · 2014
- 2 generations backK170172 UNiD Spine AnalyzerMedicrea International · 2017
- 1 generation backK180091 UNiD Spine AnalyzerMedicrea International · 2018
- This deviceK212005 UNiD Spine AnalyzerMedicrea International, Inc. · 2022
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 |
|---|---|---|---|---|---|
| −12 | K896095 | Images-on-Call Teleradiology System | Devices & Services Co. | 1990 | — |
| −11 | K962699 | Radworks Medical Imaging Software | Applicare Medical Imaging, B.V. | 1996 | — |
| −10 | K982862 | Radworks Medical Imaging Software with Quality Control Module | Applicare Medical Imaging, B.V. | 1998 | — |
| −9 | K012211 | Efilm Workstation | Efilm Medical, Inc. | 2001 | 1 |
| −8 | K020995 | Efilm Workstation with Modules | Efilm Medical, Inc. | 2002 | 2 |
| −7 | K032401 | Orthoview | Omsbar, Ltd. | 2003 | — |
| −6 | K042816 | Traumacad 1.2 | Orthocrat, Ltd. | 2004 | — |
| −5 | K073714 | Traumacad Version 2.0 | Orthocrat, Ltd. | 2008 | — |
| −4 | K111019 | Surgimap (TM) Spine | Nemaris, Inc. | 2011 | — |
| −3 | K141669 | Surgimap | Nemaris, Inc. | 2014 | — |
| −2 | K170172 | UNiD Spine Analyzer | Medicrea International | 2017 | — |
| −1 | K180091 | UNiD Spine Analyzer | Medicrea International | 2018 | — |
| 0 (this device) | K212005 | UNiD Spine Analyzer | Medicrea International, Inc. | 2022 | — |
| +1 | K251629 | UNiD™ Spine Analyzer | Medicrea International S.A.S. (Medtronic) | 2025 | — |
| +2 | K261289 | UNiD™ Spine Analyzer (SW3002) | Medicrea International S.A.S. (Medtronic) | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1991 | 2 | 0 |
| 1994 | 1 | 0 |
| 1998 | 1 | 0 |
| 2000 | 1 | 0 |
| 2001 | 3 | 0 |
| 2002 | 2 | 0 |
| 2003 | 1 | 0 |
| 2005 | 1 | 0 |
| 2007 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 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 |
|---|---|---|---|
| * | K180091 | UNiD Spine AnalyzerSummary page 5…LLZ Device Class: Class II Classification Panel: Radiology 5. Legally Marketed Predicate Device K180091, MEDICREA International, Inc. UNiD Spine Analyzer v2.0 (primary predicate). This predicate has not been subject to a design-re… | 2018 |
| † | K073291 | Capstone Spinal System | 2008 |
| † | K083026 | Clydesdale Spinal System | 2008 |
| † | K091813 | Intrepid Spinal System | 2009 |
| † | K100175 | Clydesdale Spinal System | 2010 |
| † | K110543 | Crescent (R) Spinal System Titanium | 2011 |
| † | K113528 | Clydesdale (R) Spinal System | 2011 |
| † | K120368 | Capstone Control Spinal System | 2012 |
| † | K150135 | DIVERGENCE-L Anterior/Oblique Lumbar Fusion System | 2015 |
| † | K152277 | PIVOX (tm) Oblique Lateral Spinal System | 2015 |
| † | K172199 | ELEVATE Spinal System, CAPSTONE PTC Spinal System, CRESCENT Spinal System, CRESCENT… | 2017 |
| † | K172328 | SOVEREIGN™ Spinal System | 2017 |
| † | K201267 | Adaptix Interbody System with Titan nanoLOCK Surface Technology | 2020 |
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 |
|---|---|---|---|
| K251629 | UNiD™ Spine Analyzer | 2025 | 1 |
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Dec 3, 2024 | Class II | Z-1118-2025 | Software design | Due to software anomalies that may impact on rod planning specifically, certain optional surgical parameters may have had errors that resulted i incorrect calculations displayed on system. Impacted parameters includes the following… |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 32 years and passes through 8 companies; a new generation was cleared every 2.8 years on median.
- 5 of the 25 ancestors have a recall of any class.
- Of its descendants, K251629 (Medicrea International S.A.S. (Medtronic), 2025) has gone furthest, with 1 descendant of its own.
- 2 other devices also cite its predicate K180091.
How does its category compare?
All LLZ devicesLLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, 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 UNiD™ Spine Analyzer is intended for assisting healthcare professionals in viewing and measuring images as well as planning orthopedic surgeries. The device allows surgeons and service providers to perform generic, as well as spine related measurements on images, and to plan surgical procedures. The device also includes tools for measuring anatomical components for placement of surgical implants. Clinical judgment and experience are required to properly use the software.
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/K212005 · printed Nov 6, 2026
Cite this page
510(k) Report. “K212005: UNiD Spine Analyzer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K212005
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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