Xenco Medical, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243673Xenco Medical CancelleX Cervical Interbody SystemJanuary 29, 2025
K223059Xenco Medical InterAlign Cervical Interbody SystemJune 7, 2023
K213456Xenco Medical Multilevel CerviKitDecember 21, 2021
K191074Sorrento Bone Graft SubstituteSeptember 27, 2019
K190364CancelleX Porous Titanium Lumbar Interbody DeviceApril 18, 2019
K173933Sorrento Bioglass Bone Graft SubstituteSeptember 13, 2018
K180373CancelleX Porous Titanium Lumbar Interbody DeviceAugust 24, 2018
K170611SETx Pedicle Screw SystemMay 25, 2017
K160313Xenco Medical Cervical Interbody SystemOctober 21, 2016
K161478Xenco Medical Posterior Cervical SystemSeptember 6, 2016
K160986Xenco Medical Pedicle Screw SystemMay 4, 2016
K152987Xenco Medical Cervical Interbody System, Xenco Medical Lumbar Interbody SystemDecember 11, 2015
K152302Xenco Medical Cervical Interbody System (Argus)September 10, 2015
K151733Xenco Medical Pedicle Screw SystemSeptember 4, 2015
K143158Xenco Medical Lumbar Interbody SystemMarch 20, 2015
K140786XENCO MEDICAL CERVICAL INTERBODY SYSTEMSeptember 3, 2014