50 results · 24ms · Sources: EU EUDAMED, US FDA

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PRIMACONNEX CERAMIC ABUTMENTS

FDA 510(k)
FDA Class 2 ·Dental

JOBSITE ENHANCED MOBILITY CHAIR, MODEL JEM

FDA 510(k)
FDA Class 1 ·Physical Medicine

DERMAGRIP POWDER FREE LATEX EXAMINATION GLOVES WITH ALOE VERA PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)

FDA 510(k)
FDA Class 1 ·General Hospital

VPV SYSTEM

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF MEDOS·Product code JXG·January 6, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·January 12, 2016

CODMAN VPV SYSTEM

FDA Adverse Event
Malfunction ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·January 11, 2018

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 23, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 23, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 22, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 23, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 23, 2014

CODMAN VPV SYSTEM

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·October 1, 2016

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·April 16, 2018

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·July 1, 2013

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·July 1, 2013

CODMAN VPV SYSTEM

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·November 12, 2015

CODMAN VPV SYSTEM

FDA Adverse Event
Malfunction ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·August 16, 2017

CODMAN VPV SYSTEM

FDA Adverse Event
Malfunction ·CODMAN & SHURTLEFF·Product code JXG·January 28, 2015

ADVANCE MALE SLING SYSTEM

FDA Adverse Event
Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTM·April 12, 2013

OXIMAX N-595 PULSE OXIMETER

FDA Adverse Event
Malfunction ·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code DQA·March 21, 2011