International Medical Devices Database

Data Source

Country

Device Classification

Parent Company

Name	Classification	Manufacturer	Risk Class	Country	Source
Tactys distal stem size S and M		Stryker GmbH		Sweden	SMPA
Target Nano		Stryker Neurovascular		Sweden	SMPA
V40 Unipolar heads		Stryker		Sweden	SMPA
Trident Universal Impactor/Positioner		Stryker Orthopaedics		Sweden	SMPA
HMRS distal femur resection component and HMRS distal femoral component		Howmedica Osteonics		Sweden	SMPA
HydroSet injectable bone HA substitute		Stryker Osteosynthesis Freiburg		Sweden	SMPA
LFIT Anatomic CoCr V40 Femoral Head		Stryker Orthopaedics		Sweden	SMPA
LFIT V40 taper femoral heads, V40 conical Vitallium femoral heads and PCA conical Vitallium femoral heads		Stryker Ireland		Sweden	SMPA
MEDPOR chin implant, MEDPOR BARRIER plates and MEDPOR Titanium Maximum OFW MTB		Stryker Leibinger GmbH & Co. KG		Sweden	SMPA
METS modular proximal tibial prosthesis		Stanmore Implants Worldwide		Sweden	SMPA
METS modular tumor systems product		Stanmore Implants Worldwide Limited		Sweden	SMPA
METS Principal Shaft		Stanmore Implants Worldwide Limited		Sweden	SMPA
METS Tibial Plateau Plates		Stanmore Implants		Sweden	SMPA
rhead radius head and Uni-Elbow System		Stryker GmbH		Sweden	SMPA
rHead/uHead		Stryker Trauma AG		Sweden	SMPA
T2 Knee artificial nails		Stryker Osteosynthesis		Sweden	SMPA
Device Recall GDC VORTX 2MM X 3MM	Cardiovascular Devices	Stryker Neurovascular	2	United States	USFDA
Inion CPS	Dental Devices	Stryker Craniomaxillofacial Division	2	United States	USFDA
Inion CPS Baby	Dental Devices	Stryker Craniomaxillofacial Division	2	United States	USFDA
Inion CPS Baby	Dental Devices	Stryker Craniomaxillofacial Division	2	United States	USFDA
Device Recall Vitagel	General and Plastic Surgery Devices	Orthovita, Inc., dBA Stryker Orthobiologics.	3	United States	USFDA
Device Recall MEDPOR TITAN MAX Orbital Floor and Wall (OFW) MEDPORTitaniumBarrier (MTB) Right	General and Plastic Surgery Devices	Stryker Craniomaxillofacial Division	2	United States	USFDA
Device Recall MEDPOR BARRIER Sheets Rectangle	General and Plastic Surgery Devices	Stryker Craniomaxillofacial Division	2	United States	USFDA
Device Recall MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm	General and Plastic Surgery Devices	Stryker Craniomaxillofacial Division	2	United States	USFDA
Device Recall MEDPOR BARRIER Sheets Orbital Floor Implant	General and Plastic Surgery Devices	Stryker Craniomaxillofacial Division	2	United States	USFDA

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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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