190 results · 28ms · Sources: EU EUDAMED, US FDA

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FORTITUDE CEMENT RESTRICTOR

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Q-LUX PLASMA 100 LIGHT CURE UNIT

FDA 510(k)
FDA Class 2 ·Dental

PLUS CANCELLOUS BONE SCREWS

FDA 510(k)
FDA Class 2 ·Orthopedic

SEE H10

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KXA·November 1, 2011

IN TOUCH ZU

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 26, 2013

BD VACUTAINER

FDA Adverse Event
Malfunction ·BD VACUTAINER SYSTEMS, PREANALYTICAL SOLUTIONS·Product code JKA·March 14, 2011

GE OEC 9600

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·March 19, 2008

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 16, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·November 11, 2010

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 23, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·May 9, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 18, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 16, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 2, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·October 5, 2010

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·January 10, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 17, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·March 2, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·March 14, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·June 6, 2011