52 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Sealant, Dural
FDA Pre-Market Approval
FDA Class 3
·Adherus AutoSpray Dural and ET Dural Sealant
Drug-Eluting Sinus Stent
FDA Pre-Market Approval
FDA Class 3
·Propel
Prosthesis, Metatarsophalangeal Joint Cartilage Replacement Implant
FDA Pre-Market Approval
FDA Class 3
·Cartiva Synthetic Cartilage Implant (Cartiva SCI)
Sealant, Dural
FDA Pre-Market Approval
FDA Class 3
·Adherus ET AutoSpray Dural Sealant, NUS-109
Sealant, Dural
FDA Pre-Market Approval
FDA Class 3
·DURASEAL DURAL SEALANT SYSTEM
Sealant, Dural
FDA Pre-Market Approval
FDA Class 3
·DURASEAL DURAL SEALANT SYSTEM
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Medical Adhesive Model 6517
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Lead Repair Kit Model 6946
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MynxGrip Vascular Closure Device
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX VASCULAR CLOSURE DEVICE PRODUCT FAMILY
Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation
FDA Pre-Market Approval
FDA Class 3
·Sphere-9 Mapping and Ablation Catheter, Catheter Extension Cable, Tubing Set
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·ARRAY MULTIFOCAL ULTRAVIOLET ABSORBING SILICONE POSTERIOR CHAMBER IOL
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·ALLERGAN SENSAR SOFT ACRYLIC UV-LIGHT ABSORBING POSTERIOR CHAMBER IOL
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·ULTRAVIOLET ABSORBING SILICONE POSTERIOR CHAMBER IOL'S
Scaffold, Infrapopliteal, Absorbable
FDA Pre-Market Approval
FDA Class 3
·Esprit BTK Everolimus Eluting Resorbable Scaffold System
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·ZYDERM/ZYPLAST COLLAGEN, COSMODERM/ COSMOPLAST HUMAN COLLAGEN IMPLANT
System, Photopheresis, Extracorporeal
FDA Pre-Market Approval
FDA Class 3
·THERAKOS CELLEX PHOTOPHERESIS SYSTEM
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SPECTRANETICS LASER SHEATH (SLS)
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·Pipeline Flex Embolization Device
Agent, Injectable, Embolic
FDA Pre-Market Approval
FDA Class 3
·Apollo Onyx Delivery Micro Catheter