International Medical Devices Database

Manufacturer Parent Company (2017)
Endologix Inc
Source
NOM
1 Event
- Recall of Trivascular OVation Prime 29 mm Aortic Body (Ref number TV-AB-2980-D)

One device in the database

Trivascular OVation Prime 29 mm Aortic Body (Ref number TV-AB-2980-D)

Model / Serial
Product Classification
Cardiovascular Devices
Product Description
Batch recall of the medical device "Trivascular OVation Prime 29 mm Aortic Body (Ref number TV-AB-2980-D)"

10 manufacturers with a similar name

Learn more about the data here

TriVascular Inc.

Manufacturer Parent Company (2017)
Endologix Inc.
Source
AEMPSVFOI

TriVascular

Manufacturer Parent Company (2017)
Endologix Inc.
Source
BAM

TriVascular Inc

Manufacturer Parent Company (2017)
Endologix Inc.
Source
SMPA

Trivascular, Inc

Manufacturer Address
Trivascular, Inc, 3910 Brickway Blvd, Santa Rosa CA 95403
Manufacturer Parent Company (2017)
Endologix Inc.
Source
USFDA

TriVascular, Inc.

Manufacturer Parent Company (2017)
Endologix Inc.
Source
SATP

5 more

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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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