KLS Martin Drill-Free MMF Screw— 510(k) K233721

Name: FDA 510(k) clearance K233721
Creator: U.S. Food and Drug Administration
Published: 2024-09-17

Substantially Equivalent

KLS-Martin L.P.

FDA 510(k) clearance K233721 for KLS Martin Drill-Free MMF Screw, Substantially Equivalent on 2024-09-17. Applicant: KLS-Martin L.P.. Device class: 2.

Clearance details

Applicant: KLS-Martin L.P.
Product code: Code DZL
Device class: Class 2
Regulation: 21 CFR 872.4880
Advisory panel: Dental
Date received: 2023-11-21
Decision date: 2024-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DZL

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K254286 — Guided Bone Regeneration System2026-08-24
K250123 — Master-Pin X (MP Pin with thread) (36BMP000030 / MP30)2025-09-29
K251569 — Bone Screw2025-08-13
K243190 — USTOMED Bone Fixation/Bone Augmentation Systems - PIN2025-06-27
K233419 — GBR System2025-01-03

More clearances from KLS-Martin L.P.

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K260137 — KLS Martin IPS Oral-Max Implants - MR Conditional +3 more2026-08-17
K253660 — KLS Martin Pure Pectus System2026-02-20
K254162 — KLS Martin Ixos System2026-02-20
K250988 — KLS Martin Pure Pectus System2025-12-11
K250865 — KLS Martin IPS Forearm System2025-11-14

Adverse events under product code DZL

product code DZL

Injury: 168
Total: 168

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.