510(k) Report

510(k) · Cleared

Cleared

KLS Martin Individual Patient Solutions (IPS) Planning System

K182789510(k) TraditionalCleared Mar 11, 2019161-day reviewClass II21 CFR 872.4120

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

KLS-Martin L.P. · DZJ Driver, Wire, And Bone Drill, Manual

Cleared on Mar 11, 2019 as substantially equivalent to K181241 (KLS-Martin L.P., 2018) after a 161-day review. Its family tree reaches back 6 generations to 1993. 7 later devices descend from it.

Decided
Mar 11, 2019
Review
161 days
Class
Class II
Product code
DZJ
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K924630 (1993). 11 ancestors in all, the oldest K924810 (1993). 7 later devices descend from it, 4 citing it directly.

Other ancestors, by generationDescendants, by generation 3 generations back: 2 other ancestors4 generations back: 2 other ancestors5 generations back: 1 other ancestor 1 generation forward: 4 descendants2 generations forward: 2 descendants3 generations forward: 1 descendant K181241 · KLS Martin Individual Patient Solutions (IPS) Planning System · KLS-Martin L.P. · 2018K120956 · VSP System · Medical Modeling, Inc. · 2012K060950 · 3MATIC · Materialise NV · 2006K033849 · Simplant System · Materialise NV · 2004K970617 · CT-Modeller System · Materialise NV · 1997K924630 · Surgicad (TM) View (TM) · Surgicad Corp. · 1993−50
  1. Root · 6 generations backK924630 Surgicad (TM) View (TM)Surgicad Corp. · 1993
  2. 5 generations backK970617 CT-Modeller SystemMaterialise NV · 1997
  3. 4 generations backK033849 Simplant SystemMaterialise NV · 2004
  4. 3 generations backK060950 3MATICMaterialise NV · 2006
  5. 2 generations backK120956 VSP SystemMedical Modeling, Inc. · 2012
  6. 1 generation backK181241 KLS Martin Individual Patient Solutions (IPS) Planning SystemKLS-Martin L.P. · 2018
  7. This deviceK182789 KLS Martin Individual Patient Solutions (IPS) Planning SystemKLS-Martin L.P. · 2019
  8. Descendant · cites it directly · 2 of its ownK192979 KLS Martin Individual Patient Solutions (IPS) Planning SystemKLS-Martin L.P. · 2020
  9. Descendant · cites it directly · 1 of its ownK243637 Materialise Personalized Guides and Models for Craniomaxillofacial…Materialise NV · 2025
  10. Descendant · 2 generations on · 1 of its ownK211614 CenterMed Patient Matched Assisted Surgical Planning (ASP) SystemCentermed, Inc. · 2022
  11. Descendant · 2 generations on · 0 of its ownK253308 Materialise Personalized Guides and Models for Craniomaxillofacial…Materialise NV · 2026
  12. Descendant · cites it directly · 0 of its ownK242263 TECHFIT DISRP® SystemTechfit Digital Surgery, Inc. · 2024

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2020: 12022: 12023: 22024: 12025: 12026: 1
2020high 2 (2023) · low 0 (2021)2026

Most influential descendants

Showing 5 of 7 · See all
  • K192979KLS Martin Individual Patient Solutions (IPS) Planning SystemKLS-Martin L.P. · 2020 · cites it directly2descendants
  • K243637Materialise Personalized Guides and Models for Craniomaxillofacial SurgeryMaterialise NV · 2025 · cites it directly1descendant
  • K211614CenterMed Patient Matched Assisted Surgical Planning (ASP) SystemCentermed, Inc. · 2022 · 2 generations on1descendant
  • K253308Materialise Personalized Guides and Models for Craniomaxillofacial Surgery CMF Titanium…Materialise NV · 2026 · 2 generations on0descendants
  • K242263TECHFIT DISRP® SystemTechfit Digital Surgery, Inc. · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K924630Surgicad (TM) View (TM)Surgicad Corp.1993—
−5K970617CT-Modeller SystemMaterialise NV1997—
−4K033849Simplant SystemMaterialise NV2004—
−3K0609503MATICMaterialise NV2006—
−2K120956VSP SystemMedical Modeling, Inc.2012—
−1K181241KLS Martin Individual Patient Solutions (IPS) Planning SystemKLS-Martin L.P.2018—
0 (this device)K182789KLS Martin Individual Patient Solutions (IPS) Planning SystemKLS-Martin L.P.2019—
+1K192979KLS Martin Individual Patient Solutions (IPS) Planning SystemKLS-Martin L.P.2020—
+1K243637Materialise Personalized Guides and Models for Craniomaxillofacial SurgeryMaterialise NV2025—
+2K211614CenterMed Patient Matched Assisted Surgical Planning (ASP) SystemCentermed, Inc.2022—
+2K253308Materialise Personalized Guides and Models for Craniomaxillofacial Surgery CMF…Materialise NV2026—
+1K242263TECHFIT DISRP® SystemTechfit Digital Surgery, Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
200820
201010
201110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202210
202320
202410
202510
202610
FIG. 1 — Lineage of K182789, 1993–2026Source: 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 DZJ? 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 DZJ device

  1. #1 K243637 Materialise Personalized Guides and Models for…score 13.7 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K181241KLS Martin Individual Patient Solutions (IPS) Planning System
Summary page 4
…II Product Code: DZJ, LLZ Predicate Device: KLS Martin Individual Patient Solutions (IPS) Planning System (K181241) - Primary Reference Devices: KLS Martin Individual Patient Solutions (K163579) KLS Mi…
KLS-Martin L.P.2018—
†K163579KLS Martin Individual Patient SolutionsKLS Martin L.P.2017—
†K943347KLS Mini Osteosynthesis SystemPatton, Boggs & Blow1994—
†K971297Centre-Drive Drill-Free ScrewKLS-Martin L.P.1997—

Also cleared against K181241: 2 other devices →

What descends from it? (7)

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

NumberDeviceApplicantDecidedDescendants
K192979KLS Martin Individual Patient Solutions (IPS) Planning SystemKLS-Martin L.P.20202
K243637Materialise Personalized Guides and Models for Craniomaxillofacial SurgeryMaterialise NV20251
K242263TECHFIT DISRP® SystemTechfit Digital Surgery, Inc.20240
K230276TECHFIT DISRP® SystemTechfit Digital Surgery20230

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 26 years and passes through 4 companies; a new generation was cleared every 5.8 years on median.
  • 1 of the 11 ancestors has a recall of any class.
  • Of its descendants, K192979 (KLS-Martin L.P., 2020) has gone furthest, with 2 descendants of its own.
  • 2 other devices also cite its predicate K181241.

How does its category compare?

All DZJ devices

DZJ Driver, Wire, And Bone Drill, Manual: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · DZJ

1in 2025

2012: 12014: 12015: 22018: 22019: 12020: 42021: 32022: 32023: 32024: 12025: 12026 (partial year): 2
2007high 4 (2020) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DZJ

142in 2023

2020: 379 days median2021: 403 days median2022: 179 days median2023: 142 days median
2007high 403 (2021) · low 142 (2023)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · DZJ

1in 2013

2011: 52013: 1
2007high 5 (2011) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · DZJ

14in 2025

2008: 102009: 1422010: 5172011: 5782012: 6212013: 8092014: 5392015: 182016: 162017: 92018: 82019: 42020: 172021: 222022: 232023: 222024: 132025: 14
2007high 809 (2013) · low 0 (2007)2025

MAUDE reports naming product code DZJ, 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
20070—00
20080—010
20090—0142
20100—0517
20110—5578
20121—0621
20130—1809
20141—0539
20152—018
20160—016
20170—09
20182—08
20191—04
20204379017
20213403022
20223179023
20233142022
20241—013
20251—014
20262—0—

What is it indicated for?

The KLS Martin Individual Patient Solutions (IPS) Planning System is intended for use as a software system and image segmentation system for the transfer of imaging information from a medical scanner such as a CT based system. The input data file is processed by the IPS Planning System and the result is an output data file that may then be provided as digital models or used as input to a rapid prototyping portion of the system that produces physical outputs including anatomical models, guides, splints, and case reports for use in maxillofacial surgery. The IPS Planning System is also intended as a pre-operative software tool for simulating / evaluating surgical treatment options.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K182789: KLS Martin Individual Patient Solutions (IPS) Planning System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K182789

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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