11 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GENESIS POROUS TIBIAL TRAYS & REVISION KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
3M™ Victory Series™
FDA UDI
3M UNITEK CORPORATION·00652221116673·3M™ Victory Series™ First Molar Bands, 953-274,...
ANATOMICAL SHOULDER INVERSE/REVERSE
FDA 510(k)
FDA Class 2
·Orthopedic
Med-Tainer Single Deposit Container
FDA 510(k)
FDA Class 2
·General Hospital
VIRTUOSO DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 9, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·January 7, 2011
U BY KOTEX CLICK
FDA Adverse Event
Malfunction
·AVENT S. DE R.L. DE C.V.·Product code HEB·July 23, 2014
ANATOMICAL SHOULDER REVERSE, HUMERAL CUP, 0°, RETRO
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code HSD·November 21, 2018
ANATOMICAL SHOULDER REVERSE, SCREW SYSTEM, 4.5-18
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWT·November 21, 2018
ANATOMICAL SHOULDER REVERSE, HUMERAL INSERT, PE, 36-0
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWS·November 21, 2018
ANATOMICAL SHOULDER FRACTURE, HUMERAL STEM, 7-130
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWS·November 21, 2018