Home / Companies / KLS-Martin L.P.

KLS-Martin L.P.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
58
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253660KLS Martin Pure Pectus SystemFebruary 20, 2026
K250988KLS Martin Pure Pectus SystemDecember 11, 2025
K250865KLS Martin IPS Forearm SystemNovember 14, 2025
K252573KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MMNovember 10, 2025
K233721KLS Martin Drill-Free MMF ScrewSeptember 17, 2024
K241314KLS Martin Oral-Max Implants MR Conditional (bundled)August 16, 2024
K241018KLS Martin Orthopedic Implants - MR ConditionalJuly 12, 2024
K230211CranioXpandNovember 21, 2023
K222624KLS Martin LINOS Wrist SystemMay 25, 2023
K222397KLS Martin Level One Rib Fixation SystemMarch 29, 2023
K210731KLS Martin Individual Patient SolutionsJuly 18, 2022
K210228KLS Martin IPS PreprostheticJuly 8, 2022
K210741KLS Martin Neuro RongeursJune 3, 2022
K201052KLS Martin Individual Patient Solutions (IPS) Planning SystemAugust 31, 2020
K192979KLS Martin Individual Patient Solutions (IPS) Planning SystemMarch 11, 2020
K191028KLS Martin Individual Patient SolutionsNovember 22, 2019
K182889KLS Martin Individual Patient Solutions (IPS) Planning SystemJuly 26, 2019
K182789KLS Martin Individual Patient Solutions (IPS) Planning SystemMarch 11, 2019
K181241KLS Martin Individual Patient Solutions (IPS) Planning SystemSeptember 13, 2018
K180962KLS Martin Individual Patient SolutionsAugust 13, 2018