Stryker Leibinger GmbH & Co. KG
311 devices · 1,436 adverse event reports · 6 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.
- AXS 56-19005PLATE, BONE1 report
- AXS 56-17008PLATE, BONE1 report
- NA 92-50212PLATE, BONE1 report
- Universal Mandible AXS 56-20408SCREW, FIXATION, INTRAOSSEOUS1 report
- Universal 2.0 MP AXS 56-20706SCREW, FIXATION, INTRAOSSEOUS1 report
- Universal 2.0 MP AXS 56-20705SCREW, FIXATION, INTRAOSSEOUS1 report
- Universal 2.0 MP AXS 56-20905SCREW, FIXATION, INTRAOSSEOUS1 report
- Universal Mandible AXS 56-20494SCREW, FIXATION, INTRAOSSEOUS1 report
- Universal Mandible AXS 56-20508SCREW, FIXATION, INTRAOSSEOUS1 report
- Universal Mandible AXS 56-20512SCREW, FIXATION, INTRAOSSEOUS1 report
- Universal Mandible AXS 56-20514SCREW, FIXATION, INTRAOSSEOUS1 report