510(k) Report

510(k) · Cleared

Cleared

VSP System (Titanium Palatal Splint)

K261826510(k) TraditionalCleared Jun 3, 20262-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

3D Systems, Inc. · DZJ Driver, Wire, And Bone Drill, Manual

Cleared on Jun 3, 2026 as substantially equivalent to K210347 (3D Systems, 2021) and 1 other predicate after a 2-day review. Its family tree reaches back 8 generations to 1993.

Decided
Jun 3, 2026
Review
2 days
Class
Class II
Product code
DZJ
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K924630 (1993). 13 ancestors in all, the oldest K924810 (1993). No later device cites it as a predicate yet.

  1. Root · 8 generations backK924630 Surgicad (TM) View (TM)Surgicad Corp. · 1993
  2. 7 generations backK970617 CT-Modeller SystemMaterialise NV · 1997
  3. 6 generations backK033849 Simplant SystemMaterialise NV · 2004
  4. 5 generations backK060950 3MATICMaterialise NV · 2006
  5. 4 generations backK120956 VSP SystemMedical Modeling, Inc. · 2012
  6. 3 generations backK133907 VSP SystemMedical Modeling, Inc. · 2014 · Recalled
  7. 2 generations backK192192 VSP System3D Systems · 2020
  8. 1 generation backK210347 VSP System3D Systems · 2021
  9. This deviceK261826 VSP System (Titanium Palatal Splint)3D Systems, Inc. · 2026
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K924630Surgicad (TM) View (TM)Surgicad Corp.1993—
−7K970617CT-Modeller SystemMaterialise NV1997—
−6K033849Simplant SystemMaterialise NV2004—
−5K0609503MATICMaterialise NV2006—
−4K120956VSP SystemMedical Modeling, Inc.2012—
−3K133907VSP SystemMedical Modeling, Inc.20141
−2K192192VSP System3D Systems2020—
−1K210347VSP System3D Systems2021—
0 (this device)K261826VSP System (Titanium Palatal Splint)3D Systems, Inc.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
200820
201010
201110
FIG. 1 — Lineage of K261826, 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? (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
*K210347VSP System
Summary page 5
…21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K210347 VSP System DZJ K192192…
3D Systems2021—
*K192192VSP System
Summary page 5
…Product Code K210347 VSP System DZJ K192192 VSP System DZJ Device Descr…
3D Systems2020—

What descends from it?

No later submission names this one as a predicate yet.

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 33 years and passes through 5 companies; a new generation was cleared every 5.1 years on median.
  • 2 of the 13 ancestors have a recall of any class.

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. 2026, 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 VSP® 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 VSP® 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, templates, and surgical guides for use in maxillofacial surgery. The VSP® System is also intended as a pre-operative software tool for simulating / evaluating surgical treatment options.

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. “K261826: VSP System (Titanium Palatal Splint).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K261826

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Record history
  • FDA decision record loaded Oct 30, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026