10 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
STAXX IBL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ATLANTEAN TRIGGER NEBULIZER
FDA 510(k)
FDA Class 2
·Anesthesiology
GM3 SERIES IF TENS, MODEL GM3X2IF (WHERE X IS A PARAMETER OF DIFFERENT HOUSING)
FDA 510(k)
FDA Class 2
·Neurology
AMISTEM H CEMENTLESS STEM #6 STD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL, SA·Product code MEH·February 9, 2015
AVAULTA SOLO POSTERIOR SYNTHETIC SUPPORT SYSTEM
FDA Adverse Event
Injury
·BARD SHANNON LIMITED·Product code FTL·May 16, 2013
DUROM US ACETABULAR COMPONENT 54/48 N
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·September 29, 2014
EXTENSION SET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 17, 2011
BD LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·January 4, 2026
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LKK·August 17, 2012
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 28, 2015