510(k) Report

510(k) · Cleared

Cleared

Lactosorb Push Screw

K002423510(k) TraditionalCleared Oct 20, 200073-day reviewClass II21 CFR 872.4880

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

Biomet, Inc. · DZL Screw, Fixation, Intraosseous

Cleared on Oct 20, 2000 after a 73-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Oct 20, 2000
Review
73 days
Class
Class II
Product code
DZL
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2002: 1 descendant cleared200020052010201520202025
  1. This deviceK002423 Lactosorb Push ScrewBiomet, Inc. · 2000
  2. Descendant · cites it directly · 0 of its ownK021522 Lorenz 1.5 X 4 MM Lactosorb Tap Free ScrewWalter Lorenz Surgical, Inc. · 2002

Most influential descendants

Showing 1 of 1 · See all
  • K021522Lorenz 1.5 X 4 MM Lactosorb Tap Free ScrewWalter Lorenz Surgical, Inc. · 2002 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K002423Lactosorb Push ScrewBiomet, Inc.2000—
+1K021522Lorenz 1.5 X 4 MM Lactosorb Tap Free ScrewWalter Lorenz Surgical, Inc.2002—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200210
FIG. 1 — Lineage of K002423, 2000–2002Source: 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 DZL? 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 DZL device

  1. #1 K254286 Guided Bone Regeneration Systemscore 12.2 · 2 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?

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

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K021522Lorenz 1.5 X 4 MM Lactosorb Tap Free ScrewWalter Lorenz Surgical, Inc.20020

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, K021522 (Walter Lorenz Surgical, Inc., 2002) has gone furthest, with 0 descendants of its own.

How does its category compare?

All DZL devices

DZL Screw, Fixation, Intraosseous: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DZL

4in 2025

2007: 12008: 22009: 22010: 32011: 22013: 12014: 22015: 12016: 12017: 32019: 22020: 12021: 12023: 22024: 22025: 42026 (partial year): 1
2007high 4 (2025) · low 0 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DZL

263in 2025

2010: 89 days median2017: 277 days median2025: 263 days median
2007high 277 (2017) · low 89 (2010)2026

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

Recalls per year · DZL

3in 2013

2009: 12010: 12013: 3
2007high 3 (2013) · low 0 (2007)2026

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

Adverse event reports per year · DZL

70in 2025

2007: 42008: 12009: 82010: 172011: 122012: 2362013: 1782014: 1062015: 1032016: 342017: 742018: 572019: 502020: 852021: 552022: 1622023: 1002024: 1062025: 70
2007high 236 (2012) · low 1 (2008)2025

MAUDE reports naming product code DZL, 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
20071—04
20082—01
20092—18
2010389117
20112—012
20120—0236
20131—3178
20142—0106
20151—0103
20161—034
20173277074
20180—057
20192—050
20201—085
20211—055
20220—0162
20232—0100
20242—0106
20254263070
20261—0—
Cite this page

510(k) Report. “K002423: Lactosorb Push Screw.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K002423

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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