ReLineRecalls & reported problems across all models
Nuvasive, Inc. · 129 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
ReLine models — page 2
129 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- ReLine 16025545Pedicle screw spinal system, adolescent idiopathic scoliosis1 report
- ReLine 16029590APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- ReLine 16086545Pedicle screw spinal system, adolescent idiopathic scoliosis1 report
- ReLine D10000685ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ReLine D10000745ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ReLine 13114535APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- ReLine 13114545Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ReLine 13115535ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- ReLine 13115545APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- ReLine 13116550Orthosis, spondylolisthesis spinal fixation1 report
- ReLine 13117555Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ReLine 10000831STIMULATOR, NERVE1 report
- ReLine 11455040APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- ReLine 15455300Orthosis, spondylolisthesis spinal fixation1 report
- ReLine 16460500Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ReLine 11101255ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- ReLine 11109055Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ReLine 16186535Orthosis, spondylolisthesis spinal fixation1 report
- ReLine 16186555Orthosis, spondylolisthesis spinal fixation1 report
- ReLine 10000947STIMULATOR, NERVE1 report
- ReLine 16460400APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- ReLine 10001036ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ReLine 14515530Thoracolumbosacral pedicle screw system1 report
- ReLine 14516570Appliance, fixation, spinal intervertebral body1 report
- ReLine 10001113ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ReLine 11000445Orthopedic stereotaxic instrument1 report
- ReLine 10255212APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- ReLine D10000482ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ReLine D10000800ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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