510(k) Report

510(k) · Cleared

Cleared

Modus 2.5 Mandibular Trauma Set

K992683510(k) TraditionalCleared Nov 24, 1999106-day reviewClass II21 CFR 872.4760

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

Medartis AG · JEY Plate, Bone

Cleared on Nov 24, 1999 as substantially equivalent to K950045 (Karl Leibinger GmbH U. Co. KG, 1995) and 2 other predicates after a 106-day review. Its family tree reaches back 1 generation to 1995. 2 later devices descend from it.

Decided
Nov 24, 1999
Review
106 days
Class
Class II
Product code
JEY
Recalls
None
Predicates
3

Its longest line of descent runs back 1 generation to K950045 (1995). 3 ancestors in all. 2 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1996: 1 other ancestor1995: 1 other ancestor2005: 1 descendant cleared2007: 1 descendant clearedK950045 · KLS-Martin Mandibular Fracture/Reconstruction System · Karl Leibinger GmbH U. Co. KG · 19951995200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 2 other ancestors 1 generation forward: 1 descendant2 generations forward: 1 descendant K950045 · KLS-Martin Mandibular Fracture/Reconstruction System · Karl Leibinger GmbH U. Co. KG · 19950
  1. Root · 1 generation backK950045 KLS-Martin Mandibular Fracture/Reconstruction SystemKarl Leibinger GmbH U. Co. KG · 1995
  2. This deviceK992683 Modus 2.5 Mandibular Trauma SetMedartis AG · 1999
  3. Descendant · cites it directly · 1 of its ownK050934 Modus Titanium Osteosynthesis SystemMedartis, Inc. · 2005
  4. Descendant · 2 generations on · 0 of its ownK071612 Modus Trilock 2.0/2.3/2.5Medartis AG · 2007

Most influential descendants

Showing 2 of 2 · See all
  • K050934Modus Titanium Osteosynthesis SystemMedartis, Inc. · 2005 · cites it directly1descendant
  • K071612Modus Trilock 2.0/2.3/2.5Medartis AG · 2007 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K950045KLS-Martin Mandibular Fracture/Reconstruction SystemKarl Leibinger GmbH U. Co. KG1995—
0 (this device)K992683Modus 2.5 Mandibular Trauma SetMedartis AG1999—
+1K050934Modus Titanium Osteosynthesis SystemMedartis, Inc.2005—
+2K071612Modus Trilock 2.0/2.3/2.5Medartis AG2007—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
199610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200510
200710
FIG. 1 — Lineage of K992683, 1995–2007Source: 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 JEY? 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 JEY device

  1. #1 K252246 Leforte MMF Systemscore 15.6 · 16 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? (5)

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
*K950045KLS-Martin Mandibular Fracture/Reconstruction System
Summary page 1
…fixation metallic appliances (21 CFR 888.3030) Legally Marketed Devices to which Equivalence is Claimed (Predicate Devices) KLS Martin — 2.5 Mandibular Fracture Set (K950045) W. Lorenz — 2.4 Fracture System Synthes — 2.4 Mandibular Fracture Set (K961421) Leibinger — CMF Modular Plating System Descrip…
Karl Leibinger GmbH U. Co. KG1995—
*K961421Synthes 2.4 MM Universal Locking Plate System
Summary page 1
…ch Equivalence is Claimed (Predicate Devices) KLS Martin — 2.5 Mandibular Fracture Set (K950045) W. Lorenz — 2.4 Fracture System Synthes — 2.4 Mandibular Fracture Set (K961421) Leibinger — CMF Modular Plating System Description of the Device The MODUS® 2.5 Mandibular Trauma Set is a complete fracture f…
Synthes (Usa)1996—
*K946165CMF-Titanium Cranio-Maxillo-Facial Fracture Fixation (Osteosynthesis) System
Summary page 1
…ivalence The MODUS® 2.5 Trauma Set is substantially equivalent in intended use, design, and materials to the MODUS® Titanium Osteosynthesis System previously cleared in K946165, the KLS Martin 2.5 Mandibular Fracture Set, the W. Lorenz 2.4 Fracture System, the Synthes 2.4 Mandibular Fracture Set, and the…
Elekta Instruments, Inc.1995—
*—W. Lorenz — 2.4 Fracture System
Named without a submission number
—
*—Leibinger — CMF Modular Plating System
Named without a submission number
—

Also cleared against K950045: 1 other device →

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K050934Modus Titanium Osteosynthesis SystemMedartis, Inc.20051

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?

  • None of the 3 ancestors has a recall.
  • Of its descendants, K050934 (Medartis, Inc., 2005) has gone furthest, with 1 descendant of its own.
  • 1 other device also cites its predicate K950045.

How does its category compare?

All JEY devices

JEY Plate, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JEY

2in 2025

2007: 92008: 72009: 42010: 62011: 52012: 102013: 82014: 62015: 72016: 12017: 52018: 72019: 62020: 62021: 42022: 52023: 22024: 52025: 22026 (partial year): 3
2007high 10 (2012) · low 1 (2016)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JEY

159in 2024

2007: 115 days median2008: 84 days median2009: 121 days median2010: 199 days median2011: 75 days median2012: 194 days median2013: 126 days median2014: 223 days median2015: 160 days median2017: 190 days median2018: 255 days median2019: 163 days median2020: 198 days median2021: 299 days median2022: 135 days median2024: 159 days median2026 (partial year): 258 days median
2007high 299 (2021) · low 75 (2011)2026

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

Recalls per year · JEY

1in 2020

2008: 32009: 62010: 852013: 12020: 1
2007high 85 (2010) · low 0 (2007)2026

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

Adverse event reports per year · JEY

1,003in 2025

2007: 292008: 242009: 932010: 2152011: 2412012: 4282013: 7662014: 6162015: 7672016: 5582017: 5682018: 6082019: 5952020: 6802021: 4512022: 3442023: 4952024: 6962025: 1,003
2007high 1,003 (2025) · low 24 (2008)2025

MAUDE reports naming product code JEY, 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
20079115029
2008784324
20094121693
2010619985215
20115750241
2012101940428
201381261766
201462230616
201571600767
20161—0558
201751900568
201872550608
201961630595
202061981680
202142990451
202251350344
20232—0495
202451590696
20252—01,003
202632580—

What is it indicated for?

The MODUS® 2.5 Trauma Set is intended for use in mandibular trauma fractures, e. g. in unstable, comminuted mandibular fractures and bone loss.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Also cleared against K950045

1 other device cites the same predicate.

  • K032442KLS-Martin Mandibular/Reconstruction System IIKLS-Martin L.P. · 2003

More from Medartis AG

42 FDA decisions under this applicant name. See the company

  • K260761APTUS Clavicle System 2.8Medartis AG · 2026
  • K260934TITAN Nail; APTUS K-Wire SystemMedartis AG · 2026
  • K253916APTUS Shoulder Proximal Humerus System, PentaLock 3.5Medartis AG · 2026
  • K243610APTUS Hand System; APTUS Elbow Dorsal OlecranonMedartis AG · 2025
  • K240613APTUS Elbow Dorsal Olecranon PlatesMedartis AG · 2024

Recent decisions in JEY

The JEY category page

  • K260137KLS Martin IPS Oral-Max Implants - MR Conditional; Individual Patient Solutions - Ti (IPS-Ti); Individual…KLS-Martin L.P. · 2026
  • K253206METICULY Patient-specific CMF solutionMeticuly Co., Ltd. · 2026
  • K252246Leforte MMF SystemJeil Medical Corporation · 2026
  • K253373Southern Craniomaxillofacial (CMF) SystemSouthern Medical (Pty), Ltd. · 2025
  • K251441Inion CPS 1.5 Baby Bioabsorbable Fixation System; Inion CPS 1.5/2.0/2.5 Bioabsorbable Fixation SystemInion OY · 2025

https://510kreport.com/device/K992683 · printed Nov 4, 2026

Cite this page

510(k) Report. “K992683: Modus 2.5 Mandibular Trauma Set.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K992683

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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