Synthes GmbH
5,469 devices · 68,191 adverse event reports · 12 deaths reported · 76 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.
- NA 421.535SPLATE, BONE1 report
- NA 446.10PLATE, BONE1 report
- NA 446.22PLATE, BONE1 report
- NA 446.50PLATE, BONE1 report
- NA 446.51PLATE, BONE1 report
- NA 447.042PLATE, BONE1 report
- NA 447.045PLATE, BONE1 report
- NA 447.050PLATE, BONE1 report
- NA 447.074PLATE, BONE1 report
- NA 449.110PLATE, BONE1 report
- NA 449.632PLATE, BONE1 report
- NA 460.039CERCLAGE, FIXATION1 report
- NA 460.040CERCLAGE, FIXATION1 report
- NA 487.966SCREW, FIXATION, INTRAOSSEOUS1 report
- NA 488.076EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR1 report
- NA 530.510BATH, INCUBATORS/WATER, ALL1 report
- CRANIOS Reinforced 616.05.01SMETHYL METHACRYLATE FOR CRANIOPLASTY1 report
- RapidSorb 851.002.01SPLATE, BONE1 report
- RapidSorb 851.008.01SPLATE, BONE1 report
- RapidSorb 851.421.01SPLATE, BONE1 report
- RapidSorb 851.611.01SPLATE, BONE1 report
- RapidSorb 851.711.01SPLATE, BONE1 report
- RapidSorb 851.721.01SPLATE, BONE1 report
- RapidSorb 851.724.01SPLATE, BONE1 report
- RapidSorb 851.801.01SCOVER, BURR HOLE1 report
- RapidSorb 852.264.01SPLATE, BONE1 report
- RapidSorb 852.343.01SPLATE, BONE1 report
- NA SD800.419PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.401PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.402PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.429PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.444PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.501PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.510PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.528PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.533PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.534PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.535PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD420.526PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- MATRIXWAVE 04.503.821PLATE, BONE1 report
- NA SD420.427PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD420.433PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- MatrixRIB 04.501.210.01Plate, fixation, bone1 report
- MatrixRIB 04.501.214.01Plate, fixation, bone1 report
- MatrixRIB 04.501.095Plate, fixation, bone1 report
- MatrixRIB 04.501.095SPlate, fixation, bone1 report
- MatrixRIB 04.501.104SPlate, fixation, bone1 report
- MatrixRIB 04.501.250.01Plate, fixation, bone1 report
- NA 03.315.700SCREWDRIVER, SKULLPLATE1 report
- NA SD03.505.006INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
- NA 04.501.415.01Plate, fixation, bone1 report
- NA 03.501.453Plate, fixation, bone1 report
- NA U44-640-14-02STAP, BONE1 report
- NA 04.617.816.02SIntervertebral fusion device with integrated fixation, cervical1 report
- SYNFIX Evolution 04.835.120.02SIntervertebral fusion device with integrated fixation, lumbar1 report
- NA DLS-7103-05SNEEDLE, ASPIRATION AND INJECTION, DISPOSABLE1 report
- NA 02.110.300PIN, FIXATION, SMOOTH1 report
- NA 292.30Wire, surgical1 report
- NA 292.619Screw, fixation, bone1 report
- NA 298.801.10SCERCLAGE, FIXATION1 report
- MatrixMIDFACE 04.503.204.20SCREW, FIXATION, INTRAOSSEOUS1 report
- MatrixMIDFACE 04.503.223.05PLATE, BONE1 report
- MatrixMANDIBLE 04.503.440.20PLATE, BONE1 report
- PlusDrive 400.453PLATE, BONE1 report
- NA 401.156PLATE, BONE1 report
- NA 401.158PLATE, BONE1 report
- RapidSorb 805.604.02SPLATE, BONE1 report
- RapidSorb 805.605.02SPLATE, BONE1 report
- RapidSorb 805.606.04SPLATE, BONE1 report