Xenco Medical, LLC
Xenco Medical, LLC appears in FDA public data with 0 recalls, 16 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jan 29, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 16
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K243673 | Xenco Medical CancelleX Cervical Interbody System | Jan 29, 2025 |
| K223059 | Xenco Medical InterAlign Cervical Interbody System | Jun 7, 2023 |
| K213456 | Xenco Medical Multilevel CerviKit | Dec 21, 2021 |
| K191074 | Sorrento Bone Graft Substitute | Sep 27, 2019 |
| K190364 | CancelleX Porous Titanium Lumbar Interbody Device | Apr 18, 2019 |
| K173933 | Sorrento Bioglass Bone Graft Substitute | Sep 13, 2018 |
| K180373 | CancelleX Porous Titanium Lumbar Interbody Device | Aug 24, 2018 |
| K170611 | SETx Pedicle Screw System | May 25, 2017 |
| K160313 | Xenco Medical Cervical Interbody System | Oct 21, 2016 |
| K161478 | Xenco Medical Posterior Cervical System | Sep 6, 2016 |
| K160986 | Xenco Medical Pedicle Screw System | May 4, 2016 |
| K152987 | Xenco Medical Cervical Interbody System, Xenco Medical Lumbar Interbody System | Dec 11, 2015 |
| K152302 | Xenco Medical Cervical Interbody System (Argus) | Sep 10, 2015 |
| K151733 | Xenco Medical Pedicle Screw System | Sep 4, 2015 |
| K143158 | Xenco Medical Lumbar Interbody System | Mar 20, 2015 |
| K140786 | XENCO MEDICAL CERVICAL INTERBODY SYSTEM | Sep 3, 2014 |