Spinal Elements, Inc.
24 devices · 32 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.
- KARMA 75035-175Bone Fixation Cerclage, Sublaminar3 reports
- KARMA 75311-095Orthopedic Manual Surgical Instrument3 reports
- MERCURY 63485-090Thoracolumbosacral Pedicle Screw System2 reports
- LOTUS 32545-030Appliance, Fixation, Spinal Interlaminal2 reports
- SAPPHIRE 27240-014APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY2 reports
- LUNA XD LUN20006-10Intervertebral Fusion Device With Bone Graft, Lumbar2 reports
- MERCURY 63585-080Thoracolumbosacral Pedicle Screw System1 report
- MERCURY 63595-100Thoracolumbosacral Pedicle Screw System1 report
- LOTUS 32540-028APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SAPPHIRE 26240-014APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- SAPPHIRE 27040-014APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- SAPPHIRE 27140-016APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- SAPPHIRE 27340-014APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- SAPPHIRE 27340-020APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- VERTU P52412-708Intervertebral fusion device with integrated fixation, cervical1 report
- LUCENT 11027-512Intervertebral fusion device with bone graft, lumbar1 report
- LUCENT P11351-011Intervertebral fusion device with bone graft, lumbar1 report
- LUCENT P11351-508Intervertebral fusion device with bone graft, lumbar1 report
- MERCURY 62075-050Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- MERCURY 62085-040Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- LUCENT 10010-000Orthopedic Manual Surgical Instrument1 report
- LUNA XD LUN20006-12Intervertebral Fusion Device With Bone Graft, Lumbar1 report
- Lucent XP P11350-507Intervertebral Fusion Device With Bone Graft, Lumbar1 report
- OMEGA XP 72-02Orthopedic Manual Surgical Instrument1 report