7 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ENCORE LINEAR POROUS COATED HIP
FDA 510(k)
FDA Class 2
·Orthopedic
QSI 9500
FDA 510(k)
FDA Class 2
·Neurology
AUTOCHUCK ATTACHMENT
FDA 510(k)
FDA Class 1
·Dental
M2A-MAGNUM 42-50MM TAPER INSERT-3
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·February 22, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 1, 2014
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011
InterGard Knitted Collagen Coated Vascular prostheses marketed under 510(k) # K964625; InterGard Woven Collagen Coated Vascular prostheses marketed under 510(k} #K970843 and K984294.
FDA Recall
Terminated
·Intervascular S.A.S. Zone Industrielle Athelia I La Ciotat Cedex France·Product code DSY·December 9, 2009