Medical Device Manufacturer · US , Jacksonville , FL

KLS-Martin L.P. - FDA 510(k) Cleared Devices

78 submissions · 78 cleared · Since 1994

Recent clearances: KLS Martin Pure Pectus System, KLS Martin Ixos System, KLS Martin Pure Pectus System

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78
Total
78
Cleared
0
Denied

FDA 510(k) Regulatory Record - KLS-Martin L.P. Orthopedic ✕

22 devices
1-12 of 22
Cleared Feb 20, 2026
KLS Martin Pure Pectus System
K253660 · HRS
Orthopedic · 92d
Cleared Feb 20, 2026
KLS Martin Ixos System
K254162 · HRS
Orthopedic · 60d
Cleared Dec 11, 2025
KLS Martin Pure Pectus System
K250988 · HRS
Orthopedic · 255d
Cleared Nov 14, 2025
KLS Martin IPS Forearm System
K250865 · HRS
Orthopedic · 238d
Cleared Aug 15, 2025
KLS Martin Ixos System
K250620 · HRS
Orthopedic · 168d
Cleared Jul 12, 2024
KLS Martin Orthopedic Implants - MR Conditional
K241018 · HRS
Orthopedic · 88d
Cleared May 25, 2023
KLS Martin LINOS Wrist System
K222624 · HRS
Orthopedic · 267d
Cleared Mar 29, 2023
KLS Martin Level One Rib Fixation System
K222397 · HRS
Orthopedic · 233d
Cleared Mar 28, 2023
KLS Martin Pure Pectus System
K221938 · HRS
Orthopedic · 270d
Cleared Mar 11, 2020
KLS Martin Individual Patient Solutions (IPS) Planning System
K192979 · PBF
Orthopedic · 139d
Cleared Mar 09, 2017
Level One Hand Plating System
K170124 · HRS
Orthopedic · 55d
Cleared Dec 19, 2016
KLS Martin Cannulated Headless Screws
K161259 · HWC
Orthopedic · 229d
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