699 results · 24ms · Sources: EU EUDAMED, 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