510(k) Report

510(k) · Cleared

Cleared

Steinhauser Titanium Mini Bone Plates & Screws

K862482510(k) TraditionalCleared Jul 25, 198625-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

Walter Lorenz Surgical, Inc. · JEY Plate, Bone

Cleared on Jul 25, 1986 after a 25-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 213 later devices descend from it.

Decided
Jul 25, 1986
Review
25 days
Class
Class II
Product code
JEY
Recalls
None
Predicates
0

213 later devices descend from it, 4 citing it directly.

Descendants, by year cleared 1997: 4 descendants cleared2002: 4 descendants cleared2017: 6 descendants cleared2007: 5 descendants cleared2003: 7 descendants cleared2022: 10 descendants cleared2010: 7 descendants cleared2016: 11 descendants cleared2004: 2 descendants cleared2008: 3 descendants cleared2015: 12 descendants cleared2012: 11 descendants cleared2009: 3 descendants cleared2023: 13 descendants cleared2019: 7 descendants cleared2018: 12 descendants cleared2013: 7 descendants cleared2005: 1 descendant cleared2026: 18 descendants cleared2006: 4 descendants cleared2011: 6 descendants cleared2024: 24 descendants cleared1999: 1 descendant cleared1998: 1 descendant cleared2014: 8 descendants cleared2020: 5 descendants cleared2025: 17 descendants cleared2021: 4 descendants cleared1990200020102020
  1. This deviceK862482 Steinhauser Titanium Mini Bone Plates & ScrewsWalter Lorenz Surgical, Inc. · 1986
  2. Descendant · cites it directly · 188 of its ownK963741 Leibinger Luhr Small Craniomaxillofacial Bone ScrewsHowmedica Leibinger, Inc. · 1997
  3. Descendant · cites it directly · 144 of its ownK963739 Leibinger - Luhr Small Orthopedic Bone ScrewsHowmedica Leibinger, Inc. · 1997
  4. Descendant · 2 generations on · 143 of its ownK970912 Leibinger Self-Drilling ScrewHowmedica Leibinger, Inc. · 1997
  5. Descendant · 3 generations on · 141 of its ownK974785 Auto-Drive Bone ScrewOsteomed Corp. · 1998
  6. Descendant · 4 generations on · 117 of its ownK013954 Lorenz Self Drilling ScrewsWalter Lorenz Surgical, Inc. · 2002

Showing 5 of 213 descendants. See all descendants

Descendants cleared per year

1997: 41998: 11999: 12002: 42003: 72004: 22005: 12006: 42007: 52008: 32009: 32010: 72011: 62012: 112013: 72014: 82015: 122016: 112017: 62018: 122019: 72020: 52021: 42022: 102023: 132024: 242025: 172026: 18
1997high 24 (2024) · low 0 (2000)2026

Most influential descendants

Showing 5 of 213 · See all
  • K963741Leibinger Luhr Small Craniomaxillofacial Bone ScrewsHowmedica Leibinger, Inc. · 1997 · cites it directly188descendants
  • K963739Leibinger - Luhr Small Orthopedic Bone ScrewsHowmedica Leibinger, Inc. · 1997 · cites it directly144descendants
  • K970912Leibinger Self-Drilling ScrewHowmedica Leibinger, Inc. · 1997 · 2 generations on143descendants
  • K974785Auto-Drive Bone ScrewOsteomed Corp. · 1998 · 3 generations on141descendants
  • K013954Lorenz Self Drilling ScrewsWalter Lorenz Surgical, Inc. · 2002 · 4 generations on117descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K862482Steinhauser Titanium Mini Bone Plates & ScrewsWalter Lorenz Surgical, Inc.1986—
+1K963741Leibinger Luhr Small Craniomaxillofacial Bone ScrewsHowmedica Leibinger, Inc.1997—
+1K963739Leibinger - Luhr Small Orthopedic Bone ScrewsHowmedica Leibinger, Inc.1997—
+2K970912Leibinger Self-Drilling ScrewHowmedica Leibinger, Inc.1997—
+3K974785Auto-Drive Bone ScrewOsteomed Corp.1998—
+4K013954Lorenz Self Drilling ScrewsWalter Lorenz Surgical, Inc.2002—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199740
199810
199910
200240
200370
200420
200510
200640
200750
200830
200930
201070
201160
2012110
201370
201480
2015120
2016110
201760
2018120
201970
202050
202140
2022100
2023130
2024240
2025170
2026180
FIG. 1 — Lineage of K862482, 1986–2026Source: 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), 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?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (213)

See all 213

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

NumberDeviceApplicantDecidedDescendants
K963741Leibinger Luhr Small Craniomaxillofacial Bone ScrewsHowmedica Leibinger, Inc.1997188
K963739Leibinger - Luhr Small Orthopedic Bone ScrewsHowmedica Leibinger, Inc.1997144
K022185Universal CMF SystemStryker Instruments200233
K970841Imtec/Titanium MeshImtec Corp.19972

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?

  • Of its descendants, K963741 (Howmedica Leibinger, Inc., 1997) has gone furthest, with 188 descendants of its own.

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—
Cite this page

510(k) Report. “K862482: Steinhauser Titanium Mini Bone Plates & Screws.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K862482

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026