2,364 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·TRIVASCULAR, INC. OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·UROLOGIX TARGIS SYSTEM
Implant, Hearing, Active, Middle Ear, Partially Implanted
FDA Pre-Market Approval
FDA Class 3
·MAXUM SYSTEM
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·AFX STAND-ALONE LIMB EXTENSION DELIVERY SYSTEM
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·AFX Endovascular AAA System
Sealant, Dural
FDA Pre-Market Approval
FDA Class 3
·SpineSeal Spine Sealant
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·MODEL 14760 UV ABSORBING POSTERIOR CHAMBER LENSES
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·TARGIS SYSTEM
Implant, Hearing, Active, Middle Ear, Partially Implanted
FDA Pre-Market Approval
FDA Class 3
·SOUNDTEC DIRECT IPCA SYSTEM
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·OL1000/OL1000 SC and SpinaLogic Bone Growth Stimulators
Stimulator, Invasive Bone Growth
FDA Pre-Market Approval
FDA Class 3
·SPF-4 IMPLANTABLE BONE GROWTH STIMULATOR
Filler, Bone Void, Synthetic Peptide
FDA Pre-Market Approval
FDA Class 3
·i-FACTOR Peptide Enhanced Bone Graft
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·TIER A MODELS 24050,24150,25050,25350-125 LENSES
Implant, Hearing, Active, Middle Ear, Partially Implanted
FDA Pre-Market Approval
FDA Class 3
·MAXUM
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·UROLOGIX TARGIS SYSTEM
Agent, Bulking, Injectable For Gastro-Urology Use
FDA Pre-Market Approval
FDA Class 3
·MACROPLASTIQUE IMPLANTS
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·POWERLINK SYSTEM
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·POWERLINK SYSTEMWITH INTUITRAK DELIVERY SYSTEM
Stent Graft, Bypass, Superficial Femoral Artery
FDA Pre-Market Approval
FDA Class 3
·DETOUR System
Filler, Bone Void, Synthetic Peptide
FDA Pre-Market Approval
FDA Class 3
·i-FACTOR Peptide Enhanced Bone Graft