2,109 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·PROVISC OPHTHALMIC VISCOSURGICAL DEVICE
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·AcrySof Posterior Chamber Single Piece Intraocular Lenses
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·ACRYSOF RESTOR INTRAOCULAR LENSES
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·AcrySof IQ ReSTOR Posterior Chamber Intraocular Lens
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·LADAR 6000 EXCIMER LASER SYSTEM
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·ZIRCONIA SILICATE BEAD IOL TUMBLE POLISHING
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·PROVISC OPHTHALMIC VICOSURGICAL DEVICE
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·VISCOAT(TM)
Dorsal Root Ganglion Stimulator For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·DRG Delivery Sheath
Dorsal Root Ganglion Stimulator For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Dorsal Root Ganglion (DRG) Implantable Pulse Generator (IPG)
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·ACRYSOF MONFOCAL/ACRYSOF TORIC POSTERIOR CHAMBER INTRAOCULAR LENSES/ACRYSERT DELIVERY SYSTEM
Dorsal Root Ganglion Stimulator For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Proclaim DRG IPG
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·LADAR VISION EXCIMER LASER SYSTEM
Dorsal Root Ganglion Stimulator For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Proclaim DRG IPG
Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
FDA Pre-Market Approval
FDA Class 3
·EXABLATE SYSTEM
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·ACRYSOF INTRAOCULAR LENSES
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·EON CHARGING SYSTEM
Prosthesis, Ankle, Uncemented, Non-Constrained
FDA Pre-Market Approval
FDA Class 3
·Scandinavian Total Ankle Replacment (STAR Ankle)
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·WAVELIGHT EX500 EXCIMER LASER SYSTEM, ALLEGRETTO WAVE EYE-Q EXCIMER LASER SYSTEM
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·PMMA Single-Piece Anterior Chamber Intraocular Lens