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

KLS-Martin L.P., is a surgical device manufacturer based in Jacksonville, US. The company specializes in surgical innovation across orthopedic, dental, and neurology device categories.

KLS-Martin has received 78 FDA 510(k) clearances from 78 total submissions since its first clearance in 1994. The company maintains active regulatory status, with its latest FDA 510(k) clearance in 2026. Core product areas include orthopedic implants and fixation systems, dental implants and surgical instruments, and neurosurgical devices including cranial implants and expansion systems.

Notable recent cleared devices span orthopedic trauma and reconstruction, dental surgery, and neurosurgery applications. Many products feature MR conditional technology for enhanced clinical compatibility. Explore the full clearance database to review specific device names, product codes, and clearance dates.

510(k) submissions have been managed by KLS Martin L.P. as regulatory consultant.