7 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
AUTO SUTURE ENDOSCOPIC FASCIA STAPLER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Malibu
FDA UDI
Seaspine Orthopedics Corporation·10889981080440·BONE AWL, 17mm, PALM HANDLE
VORTEX
FDA 510(k)
FDA Class 2
·Radiology
GIBRALT SPINE SYSTEMS FACET SCREW 04.0,04.5
FDA 510(k)
FDA Unclassified
·Unknown
POWERED PATIENT ROTATION BED
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code IKZ·January 11, 2013
CARPENTIER-EDWARDS PERIMOUNT MAGNA AORTIC BIOPROSTHESIS
FDA Adverse Event
Death
·EDWARDS LIFESCIENCES·Product code DYE·December 1, 2010
UNKNOWN DEPUY SZ. 52 10 DEG. DURALOC LINER
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.1818910·Product code KWA·July 3, 2014