International Medical Devices Database

Data Source

Country

Device Classification

Parent Company

Name	Classification	Manufacturer	Risk Class	Country	Source
Device Recall Ottobock Pheon 3R62 Knee Joint	Physical Medicine Devices	Otto Bock Healthcare GmbH	1	United States	USFDA
Device Recall Modular Polycentric EBS Knee Joint	Physical Medicine Devices	Otto Bock Healthcare GmbH	1	United States	USFDA
Genium X3	Physical Medicine Devices	Otto Bock Healthcare Product	2	United States	USFDA
Triton Smart Ankle	Physical Medicine Devices	Otto Bock Healthcare GmbH	1	United States	USFDA
OTTO BOCK Kenevo knee joints	Physical Medicine Devices	Otto Bock Healthcare Product	1	United States	USFDA
OTTO BOCK Kenevo knee joints	Physical Medicine Devices	Otto Bock Healthcare Product	1	United States	USFDA

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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