11 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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UNIGLIDE UNICONDYLAR KNEE PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
DRYVIEW DVM Mammography Laser Imaging Film
FDA UDI
CARESTREAM HEALTH, INC.·40889971050768·125SH 20X25CM (8X10IN) DVM(2PK) CE
NAVIPRO
FDA 510(k)
FDA Class 2
·Neurology
PEDIATRIC FIXATION RODS
FDA 510(k)
FDA Class 2
·Orthopedic
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·January 16, 2026
FATHOM GUIDEWIRE
FDA Adverse Event
Death
·BOSTON SCIENTIFIC - FREMONT·Product code DQX·June 16, 2011
RESTORE SENSOR
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LGW·April 10, 2013
RIATA ST OPTIM ACTIVE FIXATION LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008
ALTRUA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·April 12, 2011
FATHOM GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·February 23, 2010
FATHOM GUIDEWIRE
FDA Adverse Event
Injury
·SALT LAKE CITY·Product code DQX·February 23, 2010