8 results
·
27ms
·
Sources: EU EUDAMED, US FDA
CEDAR(TM) PELVIC CUSHION
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
INTERLACE MEDICAL HYSTEROSCOPIC MORCELLATION SYSTEM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Grass TWin
FDA 510(k)
FDA Class 2
·Neurology
HEARTSTREAM FR2
FDA Adverse Event
Death
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 30, 2014
PROPEX
FDA Adverse Event
Malfunction
·DENTSPLY MAILLEFER·Product code LQY·October 13, 2010
NC QUANTUM APEX¿
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·December 14, 2012
PECTUS SYSTEM ELONGAGED STABILIZER 60 X017 MM
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·February 7, 2019
SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, 17V1037, 17V2037
FDA Enforcement
Class II
·Completed·Townsend Design·January 17, 2024