Medos International Sàrl
1,963 devices · 39,868 adverse event reports · 61 deaths reported · 10 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.
- SYMPHONY 1020-21-401APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-14-240SPosterior cervical screw system1 report
- SYMPHONY 1020-21-403SPosterior cervical screw system1 report
- SYMPHONY 1020-23-103SPosterior cervical screw system1 report
- SYMPHONY 1020-21-402SPosterior cervical screw system1 report
- SYMPHONY 1020-21-401SPosterior cervical screw system1 report
- SYMPHONY 1020-30-114SPosterior cervical screw system1 report
- SYMPHONY 1020-40-328SPosterior cervical screw system1 report
- SYMPHONY 1020-35-728SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-45-226SPosterior cervical screw system1 report
- SYMPHONY 1020-50-228SPosterior cervical screw system1 report
- SYMPHONY 1020-84-600SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-64-050SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-64-055SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-35-118SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-35-120SPosterior cervical screw system1 report
- SYMPHONY 1020-50-428SPosterior cervical screw system1 report
- SYMPHONY 1020-55-234SPosterior cervical screw system1 report
- SYMPHONY 1020-35-314SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-40-112SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-40-114SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-40-122SPosterior cervical screw system1 report
- SYMPHONY 1020-40-132SPosterior cervical screw system1 report
- SYMPHONY 1020-40-134SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- VIPER PRIME 186750450SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- VIPER PRIME 186770330SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 2020-00-116CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- SYMPHONY 2020-00-134ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- SYMPHONY 2020-00-156SCREWDRIVER1 report
- SYMPHONY 2020-00-157DRIVER, PROSTHESIS1 report
- SYMPHONY 2020-00-158Orthopedic stereotaxic instrument1 report
- CONCORDE LIFT 2878-04-113ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- CONCORDE LIFT 2878-04-102ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- CONCORDE LIFT 1978-11-021CIntervertebral fusion device with bone graft, lumbar1 report
- CONCORDE LIFT 1978-11-027LIntervertebral fusion device with bone graft, lumbar1 report
- UNIVERSAL NAVIGATION EXPEDIUM 2797-02-401NOrthopedic stereotaxic instrument1 report
- SYMPHONY 2020-00-222Orthopedic stereotaxic instrument1 report
- SYMPHONY 2020-22-100ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- SYMPHONY 2020-00-503ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- SYMPHONY 2020-44-101Guide, surgical, instrument1 report
- SENTIO 286240500Neurosurgical nerve locator1 report
- N/A 302015100Orthopedic stereotaxic instrument1 report
- TELIGEN 2860-01-120RETRACTOR1 report
- NA 286004103RONGEUR1 report
- TELIGEN 286003310LAVAGE, JET1 report
- CONDUIT AET10210TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT AET10208TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT CET30101TIntervertebral fusion device with bone graft, cervical1 report
- CONDUIT LET30100TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT LET30200TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT TFT80932TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT PET21010TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT PET20910TIntervertebral fusion device with bone graft, lumbar1 report
- CONDUIT PET30200TIntervertebral fusion device with bone graft, lumbar1 report
- TELIGEN 2860-01-132TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, MANUAL1 report
- TELIGEN 2860-01-131TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, MANUAL1 report
- NA 3010-19-029Orthopedic stereotaxic instrument1 report
- NA 3010-19-030Orthopedic stereotaxic instrument1 report
- NA 3010-19-021Orthopedic stereotaxic instrument1 report
- NA 3010-19-014Orthopedic stereotaxic instrument1 report
- EXPEDIUM 179762382SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- EXPEDIUM 179789381SPedicle screw spinal system, adolescent idiopathic scoliosis1 report
- EXPEDIUM ALTALYNE VIPER 1797-96-300SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- CONDUIT 187210310Intervertebral fusion device with bone graft, lumbar1 report
- N/A 697100069SCREWDRIVER1 report
- ROBOTIC INTEGRATION INSTRUMENTS 2914-89-308Orthopedic stereotaxic instrument1 report
- TRIALTIS 5161-00-1100Orthopedic stereotaxic instrument1 report
- TRIALTIS 5161-00-1110Orthopedic stereotaxic instrument1 report
- TRIALTIS 5161-00-1120Orthopedic stereotaxic instrument1 report
- TRIALTIS 5161-00-1065Orthopedic stereotaxic instrument1 report
- TRIALTIS 5161-00-1090Orthopedic stereotaxic instrument1 report
- TRIALTIS 5161-00-0070TAP, BONE1 report
- TRIALTIS 5560-12-6045Thoracolumbosacral pedicle screw system1 report
- TRIALTIS 5560-55-4045TThoracolumbosacral pedicle screw system1 report
- TRIALTIS 5560-60-2480CThoracolumbosacral pedicle screw system1 report
- TRIALTIS 5560-60-2480TThoracolumbosacral pedicle screw system1 report
- TRIALTIS 5161-00-4080TAP, BONE1 report
- TRIALTIS 5560-12-7045CSThoracolumbosacral pedicle screw system1 report
- TRIALTIS 5560-13-8080CDThoracolumbosacral pedicle screw system1 report
- TRIALTIS 5560-13-8080DThoracolumbosacral pedicle screw system1 report
- ROBOTIC INTEGRATION INSTRUMENTS 2914-89-000Orthopedic stereotaxic instrument1 report
- TRIALTIS 5560-55-3095TThoracolumbosacral pedicle screw system1 report
- VELYS 451611002Orthopedic stereotaxic instrument1 report
- DELTAMAXX DMX180625-20Device, Vascular, for Promoting Embolization1 report
- DELTAMAXX DMX180835-20Device, Vascular, for Promoting Embolization1 report
- DELTAMAXX DMX181040-20Device, Vascular, for Promoting Embolization1 report
- DELTAMAXX DMX181650-20DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- DELTAMAXX DMX181855-20Device, Vascular, for Promoting Embolization1 report
- DELTAMAXX CERECYTE CDX180733-30Device, Vascular, for Promoting Embolization1 report
- DELTAMAXX CERECYTE CDX180935-30DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- DELTAMAXX CERECYTE CDX181445-30DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- DELTAMAXX CERECYTE CDX181855-30Device, Vascular, for Promoting Embolization1 report
- DELTAMAXX CERECYTE CDX182060-30Device, Vascular, for Promoting Embolization1 report
- ORBIT GALAXY ENPOWER XTRASOFT 641CX3505DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY ENPOWER XTRASOFT 641CX3575DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY ENPOWER XTRASOFT 641CX3509DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY ENPOWER XTRASOFT 641CX0408DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY ENPOWER XTRASOFT 641HX0206DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY ENPOWER 641CF0201DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ORBIT GALAXY ENPOWER 641CF0304DEVICE, NEUROVASCULAR EMBOLIZATION1 report