7 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OVUQUICK SELF-TEST (OVUQUICK; RAMP LH ASSAY)
FDA 510(k)
FDA Class 1
·Clinical Chemistry
ZUMA
FDA 510(k)
FDA Class 2
·Orthopedic
LapBag
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·May 13, 2019
HEARTSTART FR2
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 17, 2014
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code NBW·October 15, 2010
UNKNOWN FEMORAL KNEE STEM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·December 13, 2012