118 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PROMOGRAN MATRIX WOUND DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033565407·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033565391·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033565414·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033565421·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033565377·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033565384·
SIGN IM NAIL
FDA 510(k)
FDA Class 2
·Orthopedic
EXCELART WITH PIANISSIMO, MODEL MRT-1500/P3
FDA 510(k)
FDA Class 2
·Radiology
CURE LP
FDA UDI
MEDITECH SPINE, LLC·B167T940141290·
RESTORE ADVANCED
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·August 5, 2014
RESTORE ADVANCED
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·August 5, 2014
SURESCAN
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·July 8, 2015
RESTORE
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·August 29, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013
OPTISENSE
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011
LEAD MODEL 302
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code MUZ·March 14, 2008
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026