1,231 results · 21ms · Sources: EU EUDAMED, US FDA

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NORTH COAST BUFFERED IONTOPHORESIS ELECTRODE

FDA 510(k)
FDA Class 2 ·Physical Medicine

CUSTOM HEALTHCARE SYSTEMS, INC

FDA UDI
Manus Medical, LLC·00811870032943·

COLOR BUFFED (CB) DDH FEMORAL STEM

FDA 510(k)
FDA Class 2 ·Orthopedic

RETROGRADE CARDIOPLEGIA CANNULA, SELF-INFLATING, WITH MALLEABLE OR GUIDEWIRE STYLET

FDA 510(k)
FDA Class 2 ·Cardiovascular

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS LLC·Product code OYC·March 6, 2019

VERTECEM V+ CEMENT KIT

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code NDN·April 11, 2013

LIBERTE' MONORAIL CORONARY STENT DELIVERY SYSTEM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC·Product code MAF·May 21, 2008

ENDOTAK RELIANCE

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code NVY·April 12, 2011

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS LLC·Product code OYC·February 11, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·February 10, 2012

APPLIER, SURGICAL, CLIP

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GDO·December 30, 2016

ADMINISTRATION SET FOR HALO II AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FPA·July 17, 2019

SENSICARE SURGICAL GLOVE, SIZE 7.5.

FDA Adverse Event
Malfunction ·MEDLINE·Product code KGO·June 23, 2017

TRUE METRIX AIR

FDA Adverse Event
Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·December 4, 2019

V60 VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·September 5, 2019

V60 VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·September 5, 2019

V60 VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·September 5, 2019

V60 VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·September 5, 2019

NI

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·July 4, 2019

DORNIER COMPACT DELTA II

FDA Adverse Event
Injury ·DORNIER MEDTECH SYSTEMS GMBH·Product code LNS·July 26, 2019