Karl Leibinger Medizintechnik Gmbh & Co. Kg
FDA adverse event reports naming Karl Leibinger Medizintechnik Gmbh & Co. Kg as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: KARL LEIBINGER MEDIZINTECHNIK GMBH & CO. KG.
- Total reports
- 1,364
- Deaths
- 0
- Injuries
- 1,302
- Malfunctions
- 60
Reports per year
111
2312
3613
714
4515
6316
10017
35018
27619
15220
13121
10522
5623
1924
Source: FDA adverse event reports by year received, 2011–2024. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- External Mandibular Fixator And/Or DistractorMQN408
- Plate, Fixation, BoneHRS357
- Plate, BoneJEY280
- Bit, DrillHTW176
- Screw, Fixation, IntraosseousDZL51
- Plate, Cranioplasty, Preformed, Non-AlterableGXN27
- Implant, Endosseous, Root-FormDZE23
- Cranial Distraction SystemPBJ9
- Orthopedic Manual Surgical InstrumentLXH7
- Plate, Cranioplasty, Preformed, AlterableGWO5
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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