510(k) Report

510(k) · Cleared

Cleared

TraumaCad Mobile Release 1.0

K142923510(k) TraditionalCleared Mar 5, 2015148-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

Voyant Health, Ltd. · LLZ System, Image Processing, Radiological

Cleared on Mar 5, 2015 as substantially equivalent to K073714 (Orthocrat, Ltd., 2008) after a 148-day review. Its family tree reaches back 8 generations to 1990. 28 later devices descend from it.

Decided
Mar 5, 2015
Review
148 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K896095 (1990). 21 ancestors in all. 28 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2007: 1 other ancestor2005: 1 other ancestor2003: 1 other ancestor2002: 2 other ancestors2001: 3 other ancestors2000: 1 other ancestor1994: 1 other ancestor1998: 1 other ancestor1991: 2 other ancestors2020: 3 descendants cleared2016: 2 descendants cleared2023: 4 descendants cleared2026: 4 descendants cleared2021: 4 descendants cleared2025: 6 descendants cleared2019: 2 descendants cleared2024: 1 descendant cleared2022: 2 descendants clearedK896095 · Images-on-Call Teleradiology System · Devices & Services Co. · 1990K962699 · Radworks Medical Imaging Software · Applicare Medical Imaging, B.V. · 1996K982862 · Radworks Medical Imaging Software with Quality Control Module · Applicare Medical Imaging, B.V. · 1998K012211 · Efilm Workstation · Efilm Medical, Inc. · 2001 · recalledK020995 · Efilm Workstation with Modules · Efilm Medical, Inc. · 2002 · recalledK032401 · Orthoview · Omsbar, Ltd. · 2003K042816 · Traumacad 1.2 · Orthocrat, Ltd. · 2004K073714 · Traumacad Version 2.0 · Orthocrat, Ltd. · 20081990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 3 other ancestors4 generations back: 4 other ancestors5 generations back: 3 other ancestors6 generations back: 1 other ancestor8 generations back: 1 other ancestor 1 generation forward: 3 descendants2 generations forward: 10 descendants3 generations forward: 9 descendants4 generations forward: 6 descendants K073714 · Traumacad Version 2.0 · Orthocrat, Ltd. · 2008K042816 · Traumacad 1.2 · Orthocrat, Ltd. · 2004K032401 · Orthoview · Omsbar, Ltd. · 2003K020995 · Efilm Workstation with Modules · Efilm Medical, Inc. · 2002 · recalledK012211 · Efilm Workstation · Efilm Medical, Inc. · 2001 · recalledK982862 · Radworks Medical Imaging Software with Quality Control Module · Applicare Medical Imaging, B.V. · 1998K962699 · Radworks Medical Imaging Software · Applicare Medical Imaging, B.V. · 1996K896095 · Images-on-Call Teleradiology System · Devices & Services Co. · 1990−50
  1. Root · 8 generations backK896095 Images-on-Call Teleradiology SystemDevices & Services Co. · 1990
  2. 7 generations backK962699 Radworks Medical Imaging SoftwareApplicare Medical Imaging, B.V. · 1996
  3. 6 generations backK982862 Radworks Medical Imaging Software with Quality Control ModuleApplicare Medical Imaging, B.V. · 1998
  4. 5 generations backK012211 Efilm WorkstationEfilm Medical, Inc. · 2001 · Recalled
  5. 4 generations backK020995 Efilm Workstation with ModulesEfilm Medical, Inc. · 2002 · Recalled
  6. 3 generations backK032401 OrthoviewOmsbar, Ltd. · 2003
  7. 2 generations backK042816 Traumacad 1.2Orthocrat, Ltd. · 2004
  8. 1 generation backK073714 Traumacad Version 2.0Orthocrat, Ltd. · 2008
  9. This deviceK142923 TraumaCad Mobile Release 1.0Voyant Health, Ltd. · 2015
  10. Descendant · cites it directly · 21 of its ownK160284 JointPointJointpoint, Inc. · 2016
  11. Descendant · 2 generations on · 5 of its ownK182332 PhantomMSKOrthoGrid Systems, Inc. · 2019
  12. Descendant · 2 generations on · 4 of its ownK201928 e-Ortho Shoulder SoftwareFH Industrie · 2020
  13. Descendant · 2 generations on · 3 of its ownK203651 CuptimizeCuptimize, Inc. · 2021
  14. Descendant · 3 generations on · 3 of its ownK210136 PhantomMSK HipOrthoGrid Systems, Inc. · 2021

Showing 5 of 28 descendants. See all descendants

Descendants cleared per year

2016: 22019: 22020: 32021: 42022: 22023: 42024: 12025: 62026: 4
2016high 6 (2025) · low 0 (2017)2026

Most influential descendants

Showing 5 of 28 · See all
  • K160284JointPointJointpoint, Inc. · 2016 · cites it directly21descendants
  • K182332PhantomMSKOrthoGrid Systems, Inc. · 2019 · 2 generations on5descendants
  • K201928e-Ortho Shoulder SoftwareFH Industrie · 2020 · 2 generations on4descendants
  • K203651CuptimizeCuptimize, Inc. · 2021 · 2 generations on3descendants
  • K210136PhantomMSK HipOrthoGrid Systems, Inc. · 2021 · 3 generations on3descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K896095Images-on-Call Teleradiology SystemDevices & Services Co.1990—
−7K962699Radworks Medical Imaging SoftwareApplicare Medical Imaging, B.V.1996—
−6K982862Radworks Medical Imaging Software with Quality Control ModuleApplicare Medical Imaging, B.V.1998—
−5K012211Efilm WorkstationEfilm Medical, Inc.20011
−4K020995Efilm Workstation with ModulesEfilm Medical, Inc.20022
−3K032401OrthoviewOmsbar, Ltd.2003—
−2K042816Traumacad 1.2Orthocrat, Ltd.2004—
−1K073714Traumacad Version 2.0Orthocrat, Ltd.2008—
0 (this device)K142923TraumaCad Mobile Release 1.0Voyant Health, Ltd.2015—
+1K160284JointPointJointpoint, Inc.2016—
+2K182332PhantomMSKOrthoGrid Systems, Inc.2019—
+2K201928e-Ortho Shoulder SoftwareFH Industrie2020—
+2K203651CuptimizeCuptimize, Inc.2021—
+3K210136PhantomMSK HipOrthoGrid Systems, Inc.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199120
199410
199810
200010
200130
200220
200310
200510
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201620
201920
202030
202140
202220
202340
202410
202560
202640
FIG. 1 — Lineage of K142923, 1990–2026Source: 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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K073714Traumacad Version 2.0
Summary page 4
…LZ, Classification 21 CFR 892.2050 Name: Trade name of device: TraumaCad Mobile Release 1.0 3. Predicate TraumaCad Release 2.0 (K073714) Device: 4. Description: TraumaCad Mobile Release 1.0 allows surgeons to evaluate digita…
Orthocrat, Ltd.2008—

Also cleared against K073714: 12 other devices →

What descends from it? (28)

See all 28

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K160284JointPointJointpoint, Inc.201621
K160001TraumaCad Mobile Release 2.0Voyant Health, Ltd.20163
K202519OrthoNext Platform SystemOrthofix Srl20201

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 25 years and passes through 6 companies; a new generation was cleared every 2.8 years on median.
  • 5 of the 21 ancestors have a recall of any class.
  • Of its descendants, K160284 (Jointpoint, Inc., 2016) has gone furthest, with 21 descendants of its own.
  • 12 other devices also cite its predicate K073714.

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. 2015, 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 TraumaCad Mobile Release 1.0 program is indicated for assisting healthcare professionals in preoperative planning of orthopedic surgery. The device allows for overlaying of prosthesis templates on radiological images, and includes tools for performing measurements on the image and for positioning the template. Clinical judgment and experience are required to properly use the software. The software is not for primary image interpretation. The software is not for use on mobile phones.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K142923: TraumaCad Mobile Release 1.0.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K142923

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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