KLS-Martin L.P. - FDA 510(k) Cleared Devices
78
Total
78
Cleared
0
Denied
KLS-Martin L.P. has 78 FDA 510(k) cleared medical devices. Based in Jacksonville, US.
Latest FDA clearance: Feb 2026. Active since 1994. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by KLS-Martin L.P. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by KLS-Martin L.P.
78 devices
Cleared
Feb 20, 2026
KLS Martin Pure Pectus System
Orthopedic
92d
Cleared
Feb 20, 2026
KLS Martin Ixos System
Orthopedic
60d
Cleared
Dec 11, 2025
KLS Martin Pure Pectus System
Orthopedic
255d
Cleared
Nov 14, 2025
KLS Martin IPS Forearm System
Orthopedic
238d
Cleared
Nov 10, 2025
KLS Martin Cranial Implants - MR Conditional
Neurology
88d
Cleared
Aug 15, 2025
KLS Martin Ixos System
Orthopedic
168d
Cleared
Sep 17, 2024
KLS Martin Drill-Free MMF Screw
Dental
301d
Cleared
Aug 16, 2024
KLS Martin Oral-Max Implants MR Conditional (bundled)
Dental
98d
Cleared
Jul 12, 2024
KLS Martin Orthopedic Implants - MR Conditional
Orthopedic
88d
Cleared
Nov 21, 2023
CranioXpand
Neurology
299d
Cleared
May 25, 2023
KLS Martin LINOS Wrist System
Orthopedic
267d
Cleared
Mar 29, 2023
KLS Martin Level One Rib Fixation System
Orthopedic
233d
Looking for a specific device from KLS-Martin L.P.? Search by device name or K-number.
Search all KLS-Martin L.P. devices