Oberdorf Synthes Produktions Gmbh
FDA adverse event reports naming Oberdorf Synthes Produktions Gmbh as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: OBERDORF SYNTHES PRODUKTIONS GMBH.
- Total reports
- 16,865
- Deaths
- 20
- Injuries
- 11,456
- Malfunctions
- 5,389
Reports per year
312
15517
3,93918
7,26919
5,49820
122
Source: FDA adverse event reports by year received, 2012–2022. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Screw, Fixation, BoneHWC3,633
- Plate, Fixation, BoneHRS2,833
- Rod, Fixation, Intramedullary And AccessoriesHSB1,916
- Appliance, Fixation, Nail/Blade/Plate Combination, Multiple ComponentKTT1,262
- Orthopedic Manual Surgical InstrumentLXH693
- Plate, BoneJEY685
- Bit, DrillHTW583
- ScrewdriverHXX473
- Nail, Fixation, BoneJDS410
- Guide, Surgical, InstrumentFZX397
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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