Devices

Device Recall Endotine Transbleph 3.5

Model / Serial
Endotine Transbleph 3.5 (CFD-080-0167), Lot # 285373
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
The product was distributed in the United States and Sweden
Product Description
Endotine Transbleph 3.5 (CFD-080-0167)
Manufacturer
MicroAire Surgical Instruments, LLC
1 Event
- Recall of Device Recall Endotine Transbleph 3.5

Manufacturer

MicroAire Surgical Instruments, LLC

Manufacturer Address
MicroAire Surgical Instruments, LLC, 3590 Grand Forks Blvd, Charlottesville VA 22911-9006
Manufacturer Parent Company (2017)
Colson Associates Inc.
Source
USFDA

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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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