27 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODIFIED MOSS MIAMI 4.35MM DIAMETER POLYAXIAL SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040014523·Zirlux 16+ D3 98.5X25
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033253502·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033253472·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033253359·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033253311·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033253373·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033253434·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033253458·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033253342·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033253410·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033253397·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033253335·
VCF PERSONAL LUBRICANT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP-3BU1
FDA 510(k)
FDA Class 2
·Cardiovascular
BD DISCARDIT II SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 4, 2021
UNSPECIFIED 10ML FILL IN 10ML BD¿ PRE-FILLED NORMAL SALINE FILLED FLUSH
FDA Adverse Event
Death
·BECTON DICKINSON·Product code FOZ·April 1, 2016
IOLMASTER 500
FDA Adverse Event
Malfunction
·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·October 14, 2015
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·May 11, 2007
CONSTELLATION VISION SYSTEM
FDA Adverse Event
Injury
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·March 15, 2013