International Medical Devices Database

Manufacturer Address
Orthosensor, 1560 Sawgrass Corporate Pkwy, 4th Floor, Sunrise FL 33323-2858
Manufacturer Parent Company (2017)
OrthoSensor Inc.
Source
USFDA
1 Event
- Recall of Device Recall ORTHO SENSOR

One device in the database

Device Recall ORTHO SENSOR

Model / Serial
Version 1.82
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution including the states of CA, FL, MI and NY.
Product Description
"****ORTHO SENSOR**12-123-A Knee Trial for Trithion***1560 Saw grass Corporate Pkwy***4Th floor***Sunrise, FL 33323***www.orthosensor.com***" || Rx Only*** Sterile/EO***Made exclusively for Stryker Orthopaedics***. || Is the graphic user interface software associated with the graphic user interface, which is loaded onto the linkstations.

One manufacturer with a similar name

Learn more about the data here

Orthosensor, Inc.

Manufacturer Address
Orthosensor, Inc., 1560 Sawgrass Corporate Pkwy, 4th Floor, Sunrise FL 33323-2858
Manufacturer Parent Company (2017)
OrthoSensor Inc.
Source
USFDA

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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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