9 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
3M CURING LIGHT XL 3000
FDA 510(k)
FDA Class 2
·Dental
SwishPlus® Implant
FDA UDI
IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307106210·Ø3.7 x 8 Platform 3.5mmD
Fresh Cells
FDA UDI
DIAGNOSTIC HYBRIDS, INC.·30014613334736·SUPER E-MIX CELLS MWP W48/12F
COMPOSITE RESTORATIVE MATERIAL/RADIOPAQUE
FDA 510(k)
FDA Class 2
·Dental
K-CAP-E, STERILE
FDA 510(k)
FDA Class 2
·Orthopedic
HARMONIC SYNERGY* DISSECTING HOOK WITH TORQUE WRENCH
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 4, 2014
VERSACARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·June 23, 2014
HEARTMATE II LVAD
FDA Adverse Event
Death
·THORATEC CORP.·Product code DSQ·January 17, 2013
CAST CUTTER, 8 FOOT CORD
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code LGH·December 10, 2010