VIPERRecalls & reported problems across all models
Medos International Sàrl · 121 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
VIPER models — page 2
121 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- VIPER 186727770bone cement, posterior screw augmentation1 report
- VIPER 186727775bone cement, posterior screw augmentation1 report
- VIPER 186727860ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- VIPER 186727870ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- VIPER 186727955bone cement, posterior screw augmentation1 report
- VIPER 186727960ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- VIPER 279704100TAP, BONE1 report
- VIPER 279704900TAP, BONE1 report
- VIPER 186731550Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- VIPER 186731635APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- VIPER 186731735Orthosis, spondylolisthesis spinal fixation1 report
- VIPER 186731755APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- VIPER 186731835Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- VIPER 279704110TAP, BONE1 report
- VIPER 279704120TAP, BONE1 report
- VIPER 286715210NOrthopedic stereotaxic instrument1 report
- VIPER 286720000NOrthopedic stereotaxic instrument1 report
- VIPER 286760010NOrthopedic stereotaxic instrument1 report
- VIPER 186760130Orthosis, spondylolisthesis spinal fixation1 report
- VIPER 186760135ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- VIPER 186770135APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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