Orthosoft Inc
14 devices · 48 adverse event reports · 1 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.
- NavitrackER 20-8000-000-07Orthopedic Stereotaxic Instrument1 recall0 reports
- Fix Fluted Pin 3.2 x 150 mm Sterile 20-8000-000-10Orthopedic Stereotaxic Instrument15 reports
- ROSA® Recon 20-8020-110-01Orthopedic Stereotaxic Instrument12 reports
- Sesamoid ® 20-8000-000-11Orthopedic Stereotaxic Instrument9 reports
- Trabecular Metal 20-8075-004-01Orthopaedic Surgical Planning And Instrument Guides2 reports
- NA 20-8000-000-01Neurological Stereotaxic Instrument2 reports
- iASSIST® Knee System 20-8011-501-00Orthopedic stereotaxic instrument1 report
- ROSA® Shoulder 20-8087-400-00System, image processing, radiological1 report
- iASSIST 20-8011-002-00Orthopedic Stereotaxic Instrument1 report
- ROSA® Persona TKA cut guide - A 20-8020-007-00Orthopedic Stereotaxic Instrument1 report
- ROSA® Recon Platform 20-8020-100-01Orthopedic Stereotaxic Instrument1 report
- ROSA® KNEE OPTICAL UNIT 20-8020-120-01Orthopedic Stereotaxic Instrument1 report
- Comprehensive® Reverse Shoulder Augmented Guide and Bone Model Left 20-8090-004-01Shoulder Arthroplasty Implantation System1 report
- Comprehensive® Reverse Shoulder Augmented Guide and Bone Model Right 20-8090-004-02Shoulder Arthroplasty Implantation System1 report