10 results
·
27ms
·
Sources: EU EUDAMED, US FDA
HEADREST, PATIENT COMFORT
FDA 510(k)
FDA Class 1
·General Hospital
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011882332220·dentaform® Band, tooth 16, size 32/Roth 22
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011882332180·dentaform® Band, tooth 16, size 32/Roth 18
NUVASIVE SPHERX SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PhantomMSK
FDA 510(k)
FDA Class 2
·Radiology
PUMP MMT-522LNAL PRDGM INS CL EN ML
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code MDS·October 21, 2010
UNKNOWN DEPUY BONE SCREW
FDA Adverse Event
Injury
·DEPUY WARSAW·Product code KWA·December 20, 2012
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·June 18, 2014
EVOLUTION® MP? CS INSERT SIZE 3 STANDARD 12MM RIGH
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code HRY·December 3, 2025
EVOLUTION®MP TIB KEELED NONPOR SIZE 3 STANDARD RIG
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code HRY·December 3, 2025