7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IONTOPHORESIS DEVICE, MODIFICATION
FDA 510(k)
FDA Class 2
·Physical Medicine
Damon 3
FDA UDI
ORMCO CORPORATION·00889989003628·L4L DAMON 3 .022 -12/+2/0
MODEL #911 STEALTH MULTI PADS
FDA 510(k)
FDA Class 2
·Cardiovascular
BLADES FOR SPINAL LAMINECTOMY RETRACTOR
FDA 510(k)
FDA Class 2
·Neurology
DRILL BIT Ø1.5 L125 2FLUTE
FDA Adverse Event
Malfunction
·SYNTHES·Product code JEY·January 14, 2013
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·December 3, 2010
RIATA ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·July 3, 2014