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KLS Martin L.P.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
20
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K254162KLS Martin Ixos SystemFebruary 20, 2026
K250620KLS Martin Ixos SystemAugust 15, 2025
K221938KLS Martin Pure Pectus SystemMarch 28, 2023
K220050KLS Martin IPS DistractionAugust 11, 2022
K173320KLS Martin L1 MMF SystemFebruary 23, 2018
K163579KLS Martin Individual Patient SolutionsNovember 21, 2017
K163315Internal Distraction - SterileMay 5, 2017
K170124Level One Hand Plating SystemMarch 9, 2017
K161259KLS Martin Cannulated Headless ScrewsDecember 19, 2016
K161470Internal Distraction - SterileDecember 1, 2016
K151983KLS Martin LSS Plating SystemApril 6, 2016
K151382Patient Contoured Implant-PEEK (PCI-PEEK)November 9, 2015
K150771RxG Distraction SystemAugust 27, 2015
K141489LINOS MOH HAND PLATING SYSTEMJuly 24, 2014
K122860KLS MARTIN RECON TALONNovember 14, 2012
K083432DRILL FREE MMF SCREWMarch 31, 2009
K072764KLS MARTIN XTERNAL FIXATORDecember 20, 2007
K070169KLS MARTIN QUICK DISC, STERNAL TALON AND STERNAL PLATING - STERILEMarch 26, 2007
K062857KLS MARTIN QUICK DISCNovember 22, 2006
K060177KLS MARTIN RIGID FIXATION - STERILEApril 18, 2006