2,436 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
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
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·UROLOGIX TARGIS SYSTEM
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·ENDOLOGIX POWERLINK STENT GRAFT DELIVERY SYSTEM
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·UROLOGIX TARGIS SYSTEM
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·TIER A MODELS 24050,24150,25050,25350-125 LENSES
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·Defibtech Automated External Defibrillator (AED) Systems
Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep
FDA Pre-Market Approval
FDA Class 3
·EXOGEN 4000+
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·EXOGEN Ultrasound Bone Healing System
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·MODEL 14660 UV ABSORBING POSTERIOR CHAMBER LENSES
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·UROLOGIC TARGIS SYSTEM
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·UROLOGIC TARGIS SYSTEM
Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep
FDA Pre-Market Approval
FDA Class 3
·EXOGEN ULTRASOUND BONE HEALING SYSTEM
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·EXOGEN Ultrasound Bone Healing System