1,280 results · 21ms · Sources: EU EUDAMED, US FDA

Excimer Laser System

FDA Pre-Market Approval
FDA Class 3 ·LASERSCAN LSX EXCIMER LASER SYSTEM

Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·MODIFIED J & C LOOP POSTERIOR CHAMBER SINGLE PIECE

Dilator, Cervical, Synthetic, Osmotic, Pregnancy Termination

FDA Pre-Market Approval
FDA Class 3 ·LAMICEL(TM)

Excimer Laser System

FDA Pre-Market Approval
FDA Class 3 ·SVS APEX APEX EXIMER LASER WORKSTATION

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

FDA Pre-Market Approval
FDA Class 3 ·CORDIS PROGRAMMABLE NEURAL STIMULATOR MODELS 900A,

Excimer Laser System

FDA Pre-Market Approval
FDA Class 3 ·SVS APEX AND SVS APEX PLUS EXCIMER LASER WORKSTATIONS

Stent, Superficial Femoral Artery

FDA Pre-Market Approval
FDA Class 3 ·CORDIS SMART CONTROL VASCULAR STENT SYSTEMS

Dilator, Cervical, Synthetic, Osmotic, Pregnancy Termination

FDA Pre-Market Approval
FDA Class 3 ·LAMICEL(TM)

Implant, Intragastric For Morbid Obesity

FDA Pre-Market Approval
FDA Class 3 ·Spatz3 Adjustable Balloon System

Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·MODIFIED J-LOOP POSTERIOR CHAMBER IOL

Device, Hemostasis, Vascular

FDA Pre-Market Approval
FDA Class 3 ·Cordis Exoseal Vascular Closure Device

Stent, Superficial Femoral Artery

FDA Pre-Market Approval
FDA Class 3 ·CORDIS SMART/SMART CONTROL VASCULAR STENT SYSTEM

Lenses, Soft Contact, Extended Wear

FDA Pre-Market Approval
FDA Class 3 ·VISTAKON (SENOFILCON A) CONTACT LENS

Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·LENSTEC SOFTEC HD POSTERIOR CHAMBER INTRAOCULAR LENS

Device, Hemostasis, Vascular

FDA Pre-Market Approval
FDA Class 3 ·MYNX VASCULAR CLOSURE DEVICE

Implantable Pacemaker Pulse-Generator

FDA Pre-Market Approval
FDA Class 3 ·MAESTRO(R) SAVVI(TM) SERIES 300 VDD PACING SYSTEM

Lenses, Soft Contact, Extended Wear

FDA Pre-Market Approval
FDA Class 3 ·VISTAKON (senofilcon A) Brand Contact Lenses

Device, Hemostasis, Vascular

FDA Pre-Market Approval
FDA Class 3 ·Cordis EXOSEAL Vascular Closure Device

Stent, Carotid

FDA Pre-Market Approval
FDA Class 3 ·PRECISE Nitinol Stent System

Device, Hemostasis, Vascular

FDA Pre-Market Approval
FDA Class 3 ·MYNX VASCULAR CLOSURE DEVICE