9 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Anorganic Bone Mineral in Delivery Applicator
FDA 510(k)
FDA Class 2
·Dental
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776177188·GRAVES RIGHT OPEN VAG SPEC E-LGE
FIGURE 8 STERNOTOMY CLOSURE DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
IVIVI SOFPULSE, MODELS 912-M10, ROMA3 AND TORINO II
FDA 510(k)
FDA Class 2
·Physical Medicine
CARPENTIER-EDWARDS® PERIMOUNT® RSR PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·July 21, 2011
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 24, 2013
INRATIO PT/INR TEST STRIPS
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·July 11, 2014
TASUKI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LOX·June 6, 2019
CERAMIC ELECTRODE TIP L-HK F/GK372R
FDA Adverse Event
Injury
·AESCULAP AG·Product code GEI·July 5, 2019