8 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GMK Revision Femoral Distal Augmentation
FDA 510(k)
FDA Class 2
·Orthopedic
GMK-HINGE FEMORAL COMPONENT SIZE 2 R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KRO·June 28, 2019
GMK-HINGE FIXED TIBIAL INSERT SIZE 1/26MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KRO·July 12, 2019
U BY KOTEX CLICK UNSCENTED MENSTRUL TAMPONS
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
TIO2MESH TM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·July 15, 2011
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 11, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·September 9, 2008