7 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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HOWMEDICS DRG FEMORAL COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
SeaSpine Spacer System - Redondo™
FDA UDI
Seaspine Orthopedics Corporation·10889981045135·Redondo Trial 26mm x 24mm x 16mm, Lordotic
CARAPACE STERILE COTTON BALLS
FDA 510(k)
FDA Class 1
·General Hospital
SUTUREMATE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·January 30, 2013
COAGUCHEK® XS SYSTEM
FDA Adverse Event
Death
·ROCHE DIAGNOSTICS·Product code GJS·December 22, 2010
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 15, 2014