2,109 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·VISCOAT/DUOVISC Ophthalmic Viscoelastic System
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·AcrySof IQ ReSTOR Posterior Chamber Intraocular Lenses
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·PHYSIO-STIM & SPINAL-STIM
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·GENESIS, GENESISXP/DUAL XP, GENESISRC, GENESIS DUAL 4-CHANNEL, EON, EONC, AND EONMINI NEUROSTIMULATION (IPG) SYSTEMS
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·O2 OPTIX (LOTRAFILCON B) AND NIGHT AND DAY (LOTRAFILCON A) SOFT CONTACT LENSES FOR EXTENDED WEAR
Implant, Hearing, Active, Middle Ear, Partially Implanted
FDA Pre-Market Approval
FDA Class 3
·MAXUM SYSTEM
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Trim Change
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Genesis and EON Family Neurostimulation (IPG) System
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·AcrySof IQ ReSTOR Posterior Chamber Intraocular Lenses
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·WAVELIGHT ALLEGRETTO WAVE EXCIMER LASER SYSTEM
Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA Pre-Market Approval
FDA Class 3
·NATURAL-KNEE(R) WITH CSTI(TM)
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG)
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Prodigy, Proclaim, and Proclaim XR Spinal Cord Stimulation (SCS) Systems
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·PHYSIO-STIM MODELS 3202, 3302, 3313, 3314, 3315 AND SPINAL-STIM LODEL 2212
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·MODELS B-13F (P-10) & B-1H (P-11)
Stimulator, Autonomic Nerve, Implanted For Stroke Rehabilitation
FDA Pre-Market Approval
FDA Class 3
·Vivistim® System
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·AcrySof IQ ReSTOR Posterior Chamber Intraocular Lenses
Fluid, Intraocular
FDA Pre-Market Approval
FDA Class 3
·Perfluoron
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·IOL LENS MODEL GR1A
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·VISCOAT, DISCOCISC Ophthalmic Viscosurgical Device