Wenzel Spine, Inc.
8 devices · 16 adverse event reports · 0 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- VariLift-LX CIE3-10-28-00Intervertebral Fusion Device With Bone Graft, Lumbar5 reports
- VariLift-LX CIE3-12-24-00Intervertebral Fusion Device With Bone Graft, Lumbar3 reports
- VariLift-LX CIE3-11-24-00Intervertebral Fusion Device With Bone Graft, Lumbar2 reports
- VariLift-LX CIE3-11-28-00Intervertebral Fusion Device With Bone Graft, Lumbar2 reports
- VariLift-L CIE2-11-24-00Intervertebral Fusion Device With Bone Graft, Lumbar1 report
- VariLift-L CIE2-15-24-00Intervertebral Fusion Device With Bone Graft, Lumbar1 report
- VariLift-LX CIE3-13-24-00Intervertebral Fusion Device With Bone Graft, Lumbar1 report
- VariLift-LX CIE3-12-28-00Intervertebral Fusion Device With Bone Graft, Lumbar1 report