8 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VACON TM
FDA 510(k)
FDA Class 2
·General Hospital
Disposable Electrosurgical Pencils
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
REGENERX RINGLOC + MODULAR ACETABULAR SHELLS
FDA 510(k)
FDA Class 2
·Orthopedic
RINGLOC RIMCUP SHELL
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code LPH·August 31, 2017
MIH MOD CUP INSERTER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LXH·August 17, 2017
ONE TOUCH PING METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code NBW·May 14, 2010
HEARTSTART MRX -EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 6, 2014
UNKNOWN DEPUY PINNACLE METAL LINER
FDA Adverse Event
Injury
·DEPUY WARSAW·Product code LPH·October 3, 2012