Spineology Inc.

15 devices · 24 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.

• OptiMesh 1500 E 10-10-04-6

  Mesh, surgical, metal
  4 reports
• Fortress Pedicle Screw 10-10-48-16

  ORTHOSIS, SPINAL PEDICLE FIXATION
  3 reports
• OptiMesh Expandable Interbody Fusion System 10-10-100-4

  Intervertebral Body Graft Containment Device
  2 reports
• OptiMesh Expandable Interbody Fusion System 10-10-100-3

  Intervertebral Body Graft Containment Device
  2 reports
• OptiMesh 1500 E 10-10-04-15

  Mesh, surgical, metal
  2 reports
• Fortress Set Screw w/ Pedicle Screw 10-10-48-X

  Orthosis, spinal pedicle fixation, for degenerative disc disease
  2 reports
• OptiMesh Multiplanar Expandable Interbody Fusion System 102-47-01

  Orthopedic Manual Surgical Instrument
  1 report
• OptiMesh Expandable Interbody Fusion System 10-10-100-2

  Intervertebral Body Graft Containment Device
  1 report
• OptiMesh Multiplanar Expandable Interbody Fusion System 33-09-14

  Orthopedic Manual Surgical Instrument
  1 report
• OptiMesh 1500 E 10-10-04-8

  Mesh, surgical, metal
  1 report
• Elite Expandable Interbody Fusion Device 10-10-74-36

  Intervertebral fusion device with bone graft, lumbar
  1 report
• Elite Expandable Interbody Fusion Device 10-10-74-42

  Intervertebral fusion device with bone graft, lumbar
  1 report
• Fortress Pedicular Fixation 64-04-01

  Orthopedic Manual Surgical Instrument
  1 report
• Palisade Pedicular Fixation System 10-10-60-4

  ORTHOSIS, SPINAL PEDICLE FIXATION
  1 report
• Palisade Pedicular Fixation System 10-10-63-7

  Orthosis, spinal pedicle fixation, for degenerative disc disease
  1 report