11 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Exactech Equinoxe Reverse Shoulder Locking Cap, Exactech Equinoxe Reverse Shoulder Compression Screws, Exactech Equinoxe Reverse Shoulder Glenosphere Locking Screw
FDA 510(k)
FDA Class 2
·Orthopedic
CoRoent
FDA UDI
Nuvasive, Inc.·00887517638496·CoRoent Ant TLIF PEEK, 16x12x32mm 15°
Sonic
FDA UDI
Sonic Innovations, Inc.·05711583027203·CL80 P, VC PS BL CELEBRATE 80
Vilex Power Accessory
FDA UDI
VILEX IN TENNESSEE, INC.·00841731122285·KWire .062x9" (1.6x225mm)
FASTTAKE
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·November 19, 2001
RS-4I MUSCLE STIMULATOR FAMILY
FDA 510(k)
FDA Class 2
·Neurology
IDRIVE SYSTEM (I DRIVE POWER HANDLE, IDRIVE (RALC) SINGLE USE RELOAD)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LCS COMP RP INSERT LG+ 10MM
FDA Adverse Event
Injury
·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code NJL·July 7, 2011
PROLIFT +M PELVIC FLOOR REPAIR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTP·June 11, 2013
LIGAMAX-5MM ENDO CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC·Product code FZP·September 8, 2008
ACCUDRAIN WITH ANTI-REFLUX VALVE
FDA Adverse Event
Death
·INTEGRA NEUROSCIENCES PR·Product code JXG·November 22, 2016