124 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VERTEX RCCONSTRUCTION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code KWP·August 30, 2013
CHS
FDA UDI
Smith & Nephew, Inc.·03596010062635·COMPRESSION HIP SCREW SUPER LAG SCREW 110MM
STALIF C-Ti
FDA UDI
Centinel Spine, Inc.·00815101028842·
STALIF C
FDA UDI
Silony Medical Corp·00840402504504·STALIF C 3 Hole Domed Cage 12 X 10.5
STALIF C-Ti
FDA UDI
Centinel Spine, Inc.·00815101028637·
STALIF C
FDA UDI
Silony Medical Corp·00840402504528·STALIF C 3 Hole Tapered Cage 12 X 10.5
STALIF C
FDA UDI
Centinel Spine, Inc.·00815101023359·
STALIF C-Ti
FDA UDI
Silony Medical Corp·00840402504535·STALIF C-Ti CAGE 3 Scr tap. 12 x 10.5
STALIF C
FDA UDI
Centinel Spine, Inc.·00815101023427·
STALIF C-Ti
FDA UDI
Silony Medical Corp·00840402504511·STALIF C-Ti CAGE 3 Scr DOMED, 12 x 10.5
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383576475·Gutta Percha Points is used to root canal filin...
AUTOALIGN
FDA 510(k)
FDA Class 2
·Radiology
NAVIAID ICVI DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CATALYS SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL OPTICS·Product code OOE·March 14, 2016
CATALYS SYSTEM
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code OOE·October 30, 2015
TENDRIL STS
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·January 13, 2014
ASR UNI FEMORAL IMPL SIZE 53
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·May 20, 2013
OB TRACEVUE SERVER
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code HGM·May 4, 2011
CATALYS SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL OPTICS·Product code OOE·March 14, 2016