10,000 results
·
73ms
·
Sources: EU EUDAMED, US FDA
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