20 results · 23ms · Sources: EU EUDAMED, US FDA

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FDA 510(k)
FDA Class 2 ·Cardiovascular

Eagle Derma2 Nitrile Examination Gloves

FDA UDI
Eagle Protect Pbc·09421024254155·Derma2 Nitrile Examination Gloves, Blue, Powder...

ProLift

FDA UDI
Life Spine, Inc.·00190837117580·

ZB ProLift Narrow

FDA UDI
Life Spine, Inc.·00190837079321·

TALOS® HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B167321515120·

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B167311515120·

CAC-127-8 CARDOAC ARRAY COIL

FDA 510(k)
FDA Class 2 ·Radiology

MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, WATCHBP OFFICE TARGET (BP3MD1-4).

FDA 510(k)
FDA Class 2 ·Cardiovascular

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code NAY·January 11, 2019

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code NAY·January 11, 2019

PENUMBRA SMART COIL

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code HCG·December 11, 2015

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·March 13, 2019

UPBITING PITUITARY

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·October 8, 2014

WALLFLEX? ESOPHAGEAL

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code ESW·June 7, 2013

BIPOLAR WORKING ELEMENT

FDA Adverse Event
Malfunction ·RICHARD WOLF MEDICAL INSTRUMENTS·Product code GEI·June 23, 2011

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·April 10, 2019

ROSA ONE

FDA Adverse Event
Injury ·MEDTECH SA·Product code OLO·February 22, 2019

ROSA ONE

FDA Adverse Event
Injury ·MEDTECH SA·Product code OLO·March 11, 2019

UNK GEL BREAST IMPLANT

FDA Adverse Event
Injury ·ALLERGAN (COSTA RICA)·Product code FTR·May 27, 2020

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code NAY·April 3, 2019