42 results
·
25ms
·
Sources: EU EUDAMED, US FDA
HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP)MIC SUSCEPTIBILITY PLATES
FDA 510(k)
FDA Class 2
·Microbiology
EVOLUT FX PLUS VALVE
FDA Adverse Event
Malfunction
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·July 24, 2025
t:slim X2 Insulin Pump with Control-IQ Technology
FDA UDI
Tandem Diabetes Care, Inc.·00389152319513·Control-IQ 7.8
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033479414·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033479445·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033479469·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033479438·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033479452·
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0131150·Rocker, Hinged Locking
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033479421·
GREERTRACK SKIN TESTING SYSTEM, MODEL GT-IT, GT-IC
FDA 510(k)
FDA Class 2
·General Hospital
PREMIER ULTRASONIC SCALER AND INSERTS
FDA 510(k)
FDA Class 2
·Dental
Coral
FDA UDI
Seaspine Orthopedics Corporation·10889981111083·Cannulated Tap 9.5mm
RING ANNULOPLSTY TRICUSP CONTOUR 3D 26MM
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code KRH·July 10, 2019
PWRD ECH FLEX 60MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·March 20, 2013
SUREFIRE SCORPION NEEDLE
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRX·March 10, 2011
ICY HOT HEAT THERAPY PATCH
FDA Adverse Event
Other
·CHATTEM, INC.·Product code IMD·March 12, 2008
UNKNOWN OXFORD TIBIAL COMPONENT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JWH·February 15, 2018
UNKNOWN OXFORD TIBIAL COMPONENT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code HRY·February 15, 2018
UNKNOWN OXFORD TIBIAL COMPONENT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JWH·February 15, 2018