KLS Martin L.P.
KLS Martin L.P. appears in FDA public data with 0 recalls, 20 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 20, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 20
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K254162 | KLS Martin Ixos System | February 20, 2026 |
| K250620 | KLS Martin Ixos System | August 15, 2025 |
| K221938 | KLS Martin Pure Pectus System | March 28, 2023 |
| K220050 | KLS Martin IPS Distraction | August 11, 2022 |
| K173320 | KLS Martin L1 MMF System | February 23, 2018 |
| K163579 | KLS Martin Individual Patient Solutions | November 21, 2017 |
| K163315 | Internal Distraction - Sterile | May 5, 2017 |
| K170124 | Level One Hand Plating System | March 9, 2017 |
| K161259 | KLS Martin Cannulated Headless Screws | December 19, 2016 |
| K161470 | Internal Distraction - Sterile | December 1, 2016 |
| K151983 | KLS Martin LSS Plating System | April 6, 2016 |
| K151382 | Patient Contoured Implant-PEEK (PCI-PEEK) | November 9, 2015 |
| K150771 | RxG Distraction System | August 27, 2015 |
| K141489 | LINOS MOH HAND PLATING SYSTEM | July 24, 2014 |
| K122860 | KLS MARTIN RECON TALON | November 14, 2012 |
| K083432 | DRILL FREE MMF SCREW | March 31, 2009 |
| K072764 | KLS MARTIN XTERNAL FIXATOR | December 20, 2007 |
| K070169 | KLS MARTIN QUICK DISC, STERNAL TALON AND STERNAL PLATING - STERILE | March 26, 2007 |
| K062857 | KLS MARTIN QUICK DISC | November 22, 2006 |
| K060177 | KLS MARTIN RIGID FIXATION - STERILE | April 18, 2006 |