8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LASER PERIPHERALS INC. BARE FIBER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
P.F.C. SIGMA
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295239314·P.F.C. SIGMA TC3 TIBIAL INSERT TRIAL SZ 2 25mm ...
MICROSPAN SYSTEM
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code FED·June 8, 2006
G Surgical Marksman MIS System
FDA 510(k)
FDA Class 2
·Orthopedic
STAODYN MAX PRESET, MODEL 4470
FDA 510(k)
FDA Class 2
·Neurology
PROLIFT PELVIC FLOOR REPAIR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTP·February 14, 2013
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·January 10, 2011
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·UNKNOWN·Product code ITI·July 28, 2014