6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ULTRA-THIN DIAMOND BALLOON DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SMR Hybrid Glenoid System
FDA 510(k)
FDA Class 2
·Orthopedic
BYRON SILICONE CHIN IMPLANTS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OPTIFLUX F250NRE DIALYZER
FDA Adverse Event
Malfunction
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 19, 2014
GYNECARE GYNEMESH* PS
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTO·February 15, 2013
MILAGRO INTERFERENCE SCREW,12MM X 30MM
FDA Adverse Event
Injury
·DEPUY MITEK·Product code MBI·January 14, 2011