7 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OSTEONICS RESTORATION MONOLITHIC II SLOTTED HIP STEM SERIES
FDA 510(k)
FDA Class 2
·Orthopedic
Disposable Multistage Dilation Balloon Catheter
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
RADIANCY SKINSTATION WITH MODIFIED LIGHT UNIT ADDEMBLY
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HDI 5000 ULTRASOUND STANDARD SYSTEM
FDA Adverse Event
Malfunction
·PHILIPS ULTRASOUND, INC.·Product code IYO·March 30, 2012
CARELINK PROGRAM W/TELEMETRY C
FDA Adverse Event
Malfunction
·RICE CREEK MFG·Product code DXY·February 9, 2013
VIRTUOSO DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·January 6, 2011
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014