KLS-Martin L.P.
KLS-Martin L.P. appears in FDA public data with 0 recalls, 58 510(k) clearances, 0 FDA inspections, 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
- 58
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K253660 | KLS Martin Pure Pectus System | February 20, 2026 |
| K250988 | KLS Martin Pure Pectus System | December 11, 2025 |
| K250865 | KLS Martin IPS Forearm System | November 14, 2025 |
| K252573 | KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM | November 10, 2025 |
| K233721 | KLS Martin Drill-Free MMF Screw | September 17, 2024 |
| K241314 | KLS Martin Oral-Max Implants MR Conditional (bundled) | August 16, 2024 |
| K241018 | KLS Martin Orthopedic Implants - MR Conditional | July 12, 2024 |
| K230211 | CranioXpand | November 21, 2023 |
| K222624 | KLS Martin LINOS Wrist System | May 25, 2023 |
| K222397 | KLS Martin Level One Rib Fixation System | March 29, 2023 |
| K210731 | KLS Martin Individual Patient Solutions | July 18, 2022 |
| K210228 | KLS Martin IPS Preprosthetic | July 8, 2022 |
| K210741 | KLS Martin Neuro Rongeurs | June 3, 2022 |
| K201052 | KLS Martin Individual Patient Solutions (IPS) Planning System | August 31, 2020 |
| K192979 | KLS Martin Individual Patient Solutions (IPS) Planning System | March 11, 2020 |
| K191028 | KLS Martin Individual Patient Solutions | November 22, 2019 |
| K182889 | KLS Martin Individual Patient Solutions (IPS) Planning System | July 26, 2019 |
| K182789 | KLS Martin Individual Patient Solutions (IPS) Planning System | March 11, 2019 |
| K181241 | KLS Martin Individual Patient Solutions (IPS) Planning System | September 13, 2018 |
| K180962 | KLS Martin Individual Patient Solutions | August 13, 2018 |