7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TYPE 316L COTTER WIRE
FDA 510(k)
FDA Class 2
·Orthopedic
Arthrex®
FDA UDI
ARTHREX, INC.·00888867126084·HEADLESS COMPRES SCRW 4.3X75MM
COOPERVISION ACAP POWER DRIVE ULTRASONIC ANTERIOR
FDA 510(k)
FDA Class 2
·Ophthalmic
EIGEN FLORO-STOR FS-100
FDA 510(k)
FDA Class 2
·Radiology
EMAX 2 PLUS MOTOR
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·June 10, 2014
URETERAL INDWELLING CATHETER/STENT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SPENCER·Product code FAD·October 12, 2010
CHARGING SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 6, 2012