294 results · 19ms · Sources: EU EUDAMED, US FDA

Agent, Injectable, Embolic

FDA Pre-Market Approval
FDA Class 3 ·Onyx Liquid Embolic System

Agent, Injectable, Embolic

FDA Pre-Market Approval
FDA Class 3 ·ONYX LIQUID EMBOLIC SYSTEM

Device, Removal, Pacemaker Electrode, Percutaneous

FDA Pre-Market Approval
FDA Class 3 ·SPECTRANETICS LASER SHEATHS (SLS)

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·ACRYSOF IQ RESTOR +2.5 D MULTIFOCAL INTRAOCULAR LENS

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·TECNIS MULTIFOCAL 3-PIECE IOL

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·AMO SOFT ACRYLIC MULTIFOCAL IOLS

Agent, Injectable, Embolic

FDA Pre-Market Approval
FDA Class 3 ·ONYX LIQUID EMBOLIC SYSTEM

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·TECNIS® Multifocal Foldable Posterior Chamber IOL

Device, Removal, Pacemaker Electrode, Percutaneous

FDA Pre-Market Approval
FDA Class 3 ·SLS ll/GlideLight Catheters

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·ACRYSOF RESTOR POSTERIOR CHAMBER IOL

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·REZOOM MULTIFOCAL IOLS

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·SBL-3 Multifocal Intraocular Lens

Agent, Injectable, Embolic

FDA Pre-Market Approval
FDA Class 3 ·Apollo™ Onyx™ Delivery Micro Catheter 1.5 cm, Apollo™ Onyx™ Delivery Micro Catheter 3.0 cm

Agent, Injectable, Embolic

FDA Pre-Market Approval
FDA Class 3 ·ONYX 18LES & ONYX 34 LES

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·AcrySof ReSTOR IOLs

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·THIXO

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·ACRYSOF INTRAOCULAR LENSES

Device, Removal, Pacemaker Electrode, Percutaneous

FDA Pre-Market Approval
FDA Class 3 ·SLS SPECTRANETICS LASER SHEATHS

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·ACRYSOF RESTOR POSTERIOR CHAMBER INTRAOCULAR LENSES

Device, Removal, Pacemaker Electrode, Percutaneous

FDA Pre-Market Approval
FDA Class 3 ·Glidelight Laser Sheath