189 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AART MALAR IMPLANT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OneTouch Ultramini
FDA UDI
LifeScan Europe GmbH·00353885001281·OneTouch Ultramini Blood Glucose Monitoring Sys...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450151938·
SOLAR SHOULDER OFFSET HUMERAL HEAD
FDA 510(k)
FDA Class 2
·Orthopedic
CAVEX COLORCHANGE
FDA 510(k)
FDA Class 2
·Dental
MITEK ARTHROSCOPIC EQUIPMENT
FDA Adverse Event
Malfunction
·DEPUY MITEK·Product code LXH·March 26, 2013
MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·February 8, 2011
HIRES 90K
FDA Adverse Event
Malfunction
·ADVANCED BIONICS LLC·Product code MCM·March 24, 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