28 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Suprasorb A + Ag R
FDA 510(k)
FDA Unclassified
·Unknown
Vanguard® Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304438866·
FX V 135 stem
FDA UDI
FX SOLUTIONS·03701037315125·FX V 135 stem TA6V Ø32/08 cementless Ti/HA
REVERSE SHOULDER PROSTHESIS MONOBLOCK STEM
FDA 510(k)
FDA Class 2
·Orthopedic
SATURN ACTIVE LASER SYSTEM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
VANGUARD SERIES-A STANDARD PATELLA
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·May 9, 2018
VNGD PS TIB BRG 12X71/75MM
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018
COLLEAGUE CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 3, 2008
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CORDIS NEUROVASCULAR, INC.·Product code NJE·June 21, 2013
FLEXCATH STEERABLE SHEATH
FDA Adverse Event
Malfunction
·MEDTRONIC CRYOCATH LP·Product code DRA·July 28, 2011
BIOMET ARCOM 3 PEG/POST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018
VNGD PS TIB BRG 12X71/75MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018
BIOMET CC I-BEAM TRAY 75MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018
BIOMET FIXED CRUCIATE TIBIAL PLATE INTERLOK - WITH LOCKING BAR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 10, 2018
VANGUARD PS+ TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 10, 2018
TRUE METRIX AIR
FDA Adverse Event
Malfunction
·TRIVIDIA HEALTH INC·Product code NBW·October 12, 2021
DENALI JUGULAR SYSTEM
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 27, 2023
VANGUARD DCM PS TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·November 5, 2017
DENALI JUGULAR SYSTEM
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·November 21, 2023
DENALI FEMORAL SYSTEM
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 10, 2023