9 results
·
28ms
·
Sources: EU EUDAMED, US FDA
WIRELESS PORTABLE DETECTOR FD-W17
FDA 510(k)
FDA Class 2
·Radiology
EUROSPITAL EU-TTG IGA UMANA
FDA 510(k)
FDA Class 2
·Immunology
SCANDINAVIAN IVF SCIENCES AB, G1.2
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·December 29, 2015
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·May 2, 2013
DEPUY ASR XL FEM IMP SIZE 41
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·September 15, 2014
NAIL HOLDING SCREW, TIBIA 10 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·April 19, 2011
CANCELLO-PURE WEDGE
FDA Adverse Event
Injury
·RTI BIOLOGICS·Product code MQV·November 30, 2012
HAHN TAPERED IMPLANT Ø5.0 X 10 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·December 8, 2022