Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Xenco Medical with 16 510(k) clearances. The most recent is a 510(k) clearance dated Jan 29, 2025: Xenco Medical CancelleX Cervical Interbody System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 29, 2025 | Xenco Medical CancelleX Cervical Interbody SystemK243673 · ODP | 510(k) clearances |
| Jun 7, 2023 | Xenco Medical InterAlign Cervical Interbody SystemK223059 · OVE | 510(k) clearances |
| Dec 21, 2021 | Xenco Medical Multilevel CerviKitK213456 · KWQ | 510(k) clearances |
| Sep 27, 2019 | Sorrento Bone Graft SubstituteK191074 · MQV | 510(k) clearances |
| Apr 18, 2019 | CancelleX Porous Titanium Lumbar Interbody DeviceK190364 · MAX | 510(k) clearances |
| Sep 13, 2018 | Sorrento Bioglass Bone Graft SubstituteK173933 · MQV | 510(k) clearances |
| Aug 24, 2018 | CancelleX Porous Titanium Lumbar Interbody DeviceK180373 · MAX | 510(k) clearances |
| May 25, 2017 | SETx Pedicle Screw SystemK170611 · NKB | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
