10 results
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17ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IN-SLING
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CRYOSPRAY ABLATION SYSTEM, MODEL CC2-NAM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
FMP Extended Liners
FDA 510(k)
FDA Class 2
·Orthopedic
IBP ELBOW INTERLOK FINISH ULNAR COMPONENT STANDARD LEFT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·June 14, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·February 9, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·March 2, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·February 9, 2017
STERRAD 100NX STERILIZER
FDA Adverse Event
Malfunction
·ADVANCED STERILIZATION PRODUCTS·Product code MLR·February 21, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code LZG·January 28, 2011
M2A 1 PC SHELL 38MMX56MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·August 1, 2014