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Arthrex Inc.

Manufacturer
🇺🇸 United States·1 Importer

Arthrex Trauma, Inc., dba Advanced Orthopaedic Solutions

Manufacturer
🇺🇸 United States

Arthrex, Inc.

FDA registration
Arthrex, Inc.·103 products·🇺🇸 United States

ARTHREX, INC.

FDA registration
ARTHREX, INC.·120 products·🇺🇸 United States

Arthrex Manufacturing Inc.

FDA registration
Arthrex Manufacturing Inc.·84 products·🇺🇸 United States

ARTHREX, INC.

FDA Adverse Event
Malfunction ·BOVIE MEDICAL CORPORATION·Product code GEI·November 18, 2014

ARTHREX INC.

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MBI·December 27, 2003

ARTHREX, INC.

FDA Adverse Event
Malfunction ·BOVIE MEDICAL CORPORATION·Product code GEI·September 28, 2011

ARTHREX INC.

FDA Adverse Event
Injury ·ARTHREX INC.·Product code HRY·July 30, 1998

ARTHREX, INC

FDA Adverse Event
Injury ·ARTHREX, INC·Product code HTN·November 13, 2007

ARTHREX, INC.

FDA Adverse Event
Other ·ARTHREX, INC.·Product code MAI·June 9, 2003

ARTHREX INC.

FDA Adverse Event
Other ·ARTHREX, INC.·Product code MAI·June 9, 2003

ARTHREX, INC

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code FMI·December 29, 2011

ARTHREX, INC

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code GAB·December 29, 2011

ARTHREX, INC.

FDA Adverse Event
Injury ·BOVIE MEDICAL CORPORATION·Product code GEI·September 5, 2013

ARTHREX, INC.

FDA Adverse Event
Other ·ARTHREX, INC.·Product code MAI·June 12, 2002

ARTHREX, INC.

FDA Adverse Event
Other ·ARTHREX, INC.·Product code HRS·June 12, 2002

ARTHREX, INC.

FDA Adverse Event
Malfunction ·ARTHREX INC.·Product code HRX·September 8, 2006

ARTHREX, INC

FDA Adverse Event
Injury ·BOVIE MEDICAL CORPORATION·Product code GEI·March 13, 2015

ARTHREX, INC. SCORPION NEEDLE, KNEE

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MDM·January 2, 2024