2,375 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·EON NEUROSTIMULATION SYSTEM
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·ACRYSOF IQ ASPHERIC IOL WITH THE ULTRASERT PRELOADED DELIVERY SYSTEM
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·DURASOFT R3 (PHEMFILCON A) LENSES/SHELF LIFE
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·EON, EON MINI AND PROTEGE IPG'S
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·FOCUS(R) & NEWVUES(R) SOFT CONTACT LENSES
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·DURASOFT 3 (PHEMFILCON A) UV OPTIFIT TORIC (HYDROPHILLIC) CONTACT LENSES
Stimulator, Autonomic Nerve, Implanted For Epilepsy
FDA Pre-Market Approval
FDA Class 3
·NEUROCYBERNETIC PROSTHESIS (NCP) SYSTEM
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·WaveLight EX500 Excimer Laser System
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·AIR OPTIX plus HydraGlyde / AIR OPTIX plus HydraGlyde for Astigmatism / AIR OPTIX plus HydraGlyde Multifocal / AIR OPTIX
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·WaveLight EX500 Laser System with Patient Bed Swivel 1125
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·Provisc Ophthalmic Viscosurgical Devices
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·VISCOAT(TM)
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Proclaim family of SCS IPGs
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·POSTERIOR CHAMBER INTRAOCULAR LENSES STYLE 38XE
Ventricular (Assist) Bypass
FDA Pre-Market Approval
FDA Class 3
·EXCOR Pediatric Ventricular Assist Device
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·RESTOR POSTERIOR CHAMBER INTRAOCULAR LENSES
Dorsal Root Ganglion Stimulator For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·SlimTip DRG Trial Lead Kit, 50cm & 90cm / SlimTip DRG Implant Lead Kit, 50cm & 90cm / DRG Lead Extension Kit.
Prosthesis, Ankle, Uncemented, Non-Constrained
FDA Pre-Market Approval
FDA Class 3
·SCANDINAVIAN TOTAL ANKLE REPLACEMENT SYSTEM (S.T.A.R.ANKLE)
Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
FDA Pre-Market Approval
FDA Class 3
·EXABLATE
Implant, Hearing, Active, Middle Ear, Partially Implanted
FDA Pre-Market Approval
FDA Class 3
·MAXUM SYSTEM