39 results · 27ms · Sources: EU EUDAMED, US FDA

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K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM)

FDA 510(k)
FDA Class 2 ·Orthopedic

SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS

FDA UDI
HF ACQUISITION CO. LLC·00850065007489·

MODIFICATION TO: WINNER ST-2 STIMULATOR

FDA 510(k)
FDA Class 2 ·Physical Medicine

BIRD TBIRD LEGACY VENTILATOR

FDA 510(k)
FDA Class 2 ·Anesthesiology

NONE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·September 3, 2008

HEARTSTART MRX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·October 4, 2019

SYNCHRO 14 NEURO GUIDEWIRE

FDA Adverse Event
Injury ·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORPORATION·Product code DQX·July 24, 2007

SYRINGE CONTROL 10ML LL BNS

FDA Adverse Event
Injury ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 5, 2019

10 ML BD LUER-LOK CONTROL SYRINGE

FDA Adverse Event
Injury ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 5, 2019

SYNCHRO -10 NEURO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIV·Product code DQX·December 15, 2006

SYNCHRO-14 NEURO GUIDEWIRE

FDA Adverse Event
Malfunction ·NEUROVASCULAR , A DIV. OF BOSTON SCIENTIFIC CORP·Product code DQX·December 19, 2006

SYNCHRO 14 GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP.·Product code DQX·September 20, 2007

SYNCHRO .014 GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP. / NEUROCASCULAR DIVISION·Product code DQX·August 16, 2007

SYNCHRO .014 GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP. / NEUROVASCULAR DIV.·Product code DQX·August 16, 2007

SYNCHRO -14 NEURO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIVISION·Product code DQX·November 30, 2006

SYNCHRO-14 NEURO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code DQX·September 12, 2007

SYNCHRO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQX·October 16, 2009

CARTO® 3 SYSTEM

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER, LTD (HAIFA, ISRAEL)·Product code DQK·March 27, 2013

TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·March 18, 2011

ACRYSOF

FDA Adverse Event
Other ·ALCON RESEARCH, LTD/HUNTINGTON·Product code HQL·March 21, 2008