915 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·NOVOTTF-100A SYSTEM
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·OPTUNE (FORMERLY THE NOVOTTF-100A SYSTEM)
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·Optune System
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·OPTUNE
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·Optune
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·Optune® Gio
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·Optune
MOTIONSPECT
FDA 510(k)
FDA Class 3
·Unknown
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·IOL
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SOFTEC HD INTRAOCULAR LENS (IOL), SOFTEC I IOL, SOFTEC HD PS IOL
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SOFTEC HD INTRAOCULAR LENS (IOL)/SOFTEC I IOL/SOFTEC HD PS IOL
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SENSAR 1-Piece IOL; TECNIS 1-Piece IOL; TECNIS 1-Piece OptiBlue IOL; Preloaded TECNIS 1-Piece IOL
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·ARRAY MULTIFOCAL IOLS & REZOOM MULTIFOCAL IOLS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·ACRYSOF TORIC POSTERIOR CHANBER IOL, ACRYSOF TORIC SINGLE-PIECE NATURAL IOL, ACRYSOF IQ TORIC IOL & ACRYSOF TORIC IOL
Device, Testicular Hypothermia
FDA Pre-Market Approval
FDA Class 3
·REPRO-MED - THD
Ligaments And Tendons, Synthetic
FDA Pre-Market Approval
FDA Class 3
·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE
Device, Testicular Hypothermia
FDA Pre-Market Approval
FDA Class 3
·REPRO-MED - THD ADDRESS CHANGE / MANU. FACILITY
Ligaments And Tendons, Synthetic
FDA Pre-Market Approval
FDA Class 3
·CENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE
Ligaments And Tendons, Synthetic
FDA Pre-Market Approval
FDA Class 3
·STRKYER KNEE AUGMENTATION GRAFT
Ligaments And Tendons, Synthetic
FDA Pre-Market Approval
FDA Class 3
·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE