9 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FLOW-DIRECTED THERMODILUTION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
ERA® Implant Abutment Micro 0°, 4mm Cuff (X)
FDA UDI
STERNGOLD DENTAL LLC·00841549104725·Implant retained overdentures are an establishe...
Cortera
FDA UDI
Xtant Medical Holdings, Inc.·00840311234004·Tap, NAV, Open Cann, 8.0
NA
FDA UDI
aap Implantate AG·04042409452468·Double Drill Guide Ø1.6/Ø3.7
SYMMETRIC UNICOMPARTMENTAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SUNTOUCH TOPICAL HEMOSTATIC DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
CODEMASTER XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 25, 2014
SENSIA SR
FDA Adverse Event
Malfunction
·MEDTRONIC S.A.·Product code NVZ·October 31, 2012
DORNIER HOLMIUM LASER FIBER
FDA Adverse Event
Malfunction
·DORNIER MEDTECH AMERICA, INC.·Product code GEX·July 21, 2010