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. Dental ✕

42 devices

1-12 of 42

Cleared Sep 17, 2024

KLS Martin Drill-Free MMF Screw

Cleared Aug 16, 2024

KLS Martin Oral-Max Implants MR Conditional (bundled)

Cleared Aug 11, 2022

KLS Martin IPS Distraction

Cleared Jul 18, 2022

KLS Martin Individual Patient Solutions

Cleared Jul 08, 2022

KLS Martin IPS Preprosthetic

Cleared Nov 22, 2019

KLS Martin Individual Patient Solutions

Cleared Mar 11, 2019

KLS Martin Individual Patient Solutions (IPS) Planning System

Cleared Sep 13, 2018

KLS Martin Individual Patient Solutions (IPS) Planning System

Cleared Aug 13, 2018

KLS Martin Individual Patient Solutions

Cleared Feb 23, 2018

KLS Martin L1 MMF System

Cleared Nov 21, 2017

KLS Martin Individual Patient Solutions

Cleared Dec 01, 2016

Internal Distraction - Sterile

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