22 results
·
34ms
·
Sources: EU EUDAMED, US FDA
COBE SMARXT OPTIMIN SURFACE MODIFIED HOLLOW FIBER MEMBRANE OXYGENATOR
FDA 510(k)
FDA Class 2
·Cardiovascular
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012672·PedFuse Remind LES, Quad, 7.0mm x 80mm
SONOMA
FDA UDI
FGX INTERNATIONAL INC.·00193033496374·
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0134080·Trial, TLIF, 27L OB STR 7Deg, 8mm
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0134100·Trial, TLIF, 27L OB STR 7Deg, 10mm
VIVA
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
BIOFIND
FDA 510(k)
FDA Class 2
·Neurology
M2A-38 CUP NON FLARED SZ 54MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·March 20, 2013
ANT-CER 2 LVL PLATE ASSY, 40MM
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code KWQ·February 3, 2011
ENTRUST AT
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·March 10, 2008
ACT ARTIC E1 HIP BRG 28X54MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWY·May 30, 2019
CER BIOLOXD MOD HD 28MM -3 NK
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·May 30, 2019
G7 OSSEOTI MULTIHOLE 66MM I
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·May 30, 2019
SERIES A PATELLA
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·November 29, 2017
REGENEREX TIBIAL TRAY
FDA Adverse Event
Injury
·.·Product code MBH·November 29, 2017
VANGUARD FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·November 29, 2017
MAXIM FINNED STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·November 29, 2017
ACCESS® 2 IMMUNOASSAY CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHA·January 7, 2012
VANGUARD PS OPEN BOX FEMORAL POROUS COAT/ BOND COAT 62.5MM RIGHT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·November 2, 2017
RGX 3 PEG SER A PATELLA 34MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBH·July 10, 2017