10 results
·
27ms
·
Sources: EU EUDAMED, US FDA
LAPAROSCOPY DRAPE, BOUNDARY
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
ANKLE HINDFOOT NAILING SYSTEM
FDA UDI
ORTHOFIX SRL·18053340347372·ANKLE HINDFOOT REVISION NAIL TI L300MM D12MM ST...
5MM PROTEGE EVERFLEX SELF EXPANDING BILIARY STENT SYSTEM, MODEL PRP35-05
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Mako Partial Knee Application
FDA 510(k)
FDA Class 2
·Neurology
PERMOBIL
FDA Adverse Event
Malfunction
·PERMOBIL INC.·Product code ITI·March 26, 2014
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·October 4, 2012
SERIES 20000 LEGACY
FDA Adverse Event
Injury
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·July 23, 2010
4.3MM THREADED LCP(TM) DRILL GUIDE
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code FZX·November 14, 2018
4.3MM THREADED LCP(TM) DRILL GUIDE
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code FZX·November 14, 2018
4.3MM THREADED LCP(TM) DRILL GUIDE
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code FZX·November 14, 2018