International Medical Devices Database

Manufacturer Address
Acclarent, Inc., 1525B Obrien Dr, Menlo Park CA 94025-1463
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA
1 Event
- Recall of RELIEVA FLEX Sinus Guide Catheter

One device in the database

RELIEVA FLEX Sinus Guide Catheter

Model / Serial
Catalog number GC070RF, Lot 120709i-cm, Expiry 7/31/2014.
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
US in the state of Texas
Product Description
RELIEVA FLEX Sinus Guide Catheter F-70. || Catalog number GC070RF. || Product Usage - Sinus Catheter - Intended to provide a means to access the sinus space for diagnostic and therapeutic procedures. || .

2 manufacturers with a similar name

Learn more about the data here

Acclarent, Inc.

Manufacturer Address
Acclarent, Inc., 1525b Obrien Dr, Menlo Park CA 94025-1463
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA

Acclarent, Inc.

Manufacturer Address
Acclarent, Inc., 1525-B O'Brien Dr, Menlo Park CA 94025-1463
Manufacturer Parent Company (2017)
Johnson & Johnson
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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