699 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Scheker DRUJ
FDA UDI
APTIS MEDICAL, LLC·B013DRUJKWD0·K-Wire Dispenser 6 3/4"
BIOPRO GREAT TOE MP JOINT
FDA Adverse Event
Injury
·BIOPRO, INC.·Product code KWD·May 15, 2014
UNK
FDA Adverse Event
Malfunction
·UNK·Product code KWD·March 18, 2004
ANGLED SMART TOE IMPLANT
FDA Adverse Event
Injury
·MEMOMETAL INC·Product code KWD·May 6, 2010
SWANSON GREAT TOE IMPLANT WITH GROMMETS
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWD·January 16, 2004
ANATOEMIC, 20 MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWD·October 7, 2014
HEMICAP® MTP RESURFACING HEMI-ARTHROPLASTY IMPLANT
FDA Adverse Event
Injury
·ARTHROSURFACE, INC.·Product code KWD·December 26, 2017
CAP GREAT TOE RESURFACING HEMI-ARTHROPLASTY IMPLANT
FDA Adverse Event
Injury
·ARTHROSURFACE, INC.·Product code KWD·October 17, 2017
HEMICAP® TOE DF & TOEMOTION® IMPLANT SYSTEMS
FDA Adverse Event
Malfunction
·ARTHROSURFACE·Product code KWD·May 20, 2022
SILASTIC GREAT TOE IMPLANT
FDA Adverse Event
Injury
·DOW CORNING CORPORATION·Product code KWD·March 14, 2002
MOVEMENT GREAT TOE INSTRUMENTS
FDA Adverse Event
Malfunction
·ASCENSION ORTHOPEDICS·Product code KWD·March 15, 2012
P.C.A HIP SYSTEM ACETABULAR INSERT SIZE D 32MM/D
FDA Adverse Event
Injury
·HOWMEDICA/DAVIS-COUPENS & ASSOC.·Product code KWD·June 12, 1996
LPT GREAT TOE IMPLANT
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWD·July 24, 2015
HEMICAP TOE IMPLANT
FDA Adverse Event
Injury
·ARTHROSURFACE·Product code KWD·August 21, 2015
UNKNOWN_SELZACH_PRODUCT
FDA Adverse Event
Injury
·STRYKER GMBH·Product code KWD·July 13, 2015
ANATOEMIC, 18.5MM
FDA Adverse Event
Injury
·ARTHREX INC.·Product code KWD·November 21, 2017
HEMICAP® MTP RESURFACING HEMI-ARTHROPLASTY IMPLANT
FDA Adverse Event
Injury
·ARTHROSURFACE, INC.·Product code KWD·October 25, 2017
SWANSON GREAT TOE IMPLANT
FDA Adverse Event
Injury
·WRIGHT MEDICAL CORP·Product code KWD·October 10, 2003
SWANSON FLEXIBLE HINGE TOE WITH GROMMETS
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWD·July 16, 2015
VILEX IMPLANT
FDA Adverse Event
Malfunction
·VILEX IN TENNESSEE, INC.·Product code KWD·November 15, 2017