10,000 results
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50ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Wearable Automated External Defibrillator
FDA Pre-Market Approval
FDA Class 3
·LifeVest Wearable Defibrillator
Stent, Superficial Femoral Artery
FDA Pre-Market Approval
FDA Class 3
·EverFlex Self-Expanding Peripheral Stent System; EverFlex Self-Expanding Peripheral Stent with Entrust Delivery System;
Stent, Superficial Femoral Artery
FDA Pre-Market Approval
FDA Class 3
·Gore Tigris Vascular Stent
Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·Oxford Patrial Knee System
Implanted Brain Stimulator For Epilepsy
FDA Pre-Market Approval
FDA Class 3
·NeuroPace RNS System
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·EluNIR Ridaforolimus Eluting Coronary Stent System
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·Catheter RF Contactr, Catheter RF Enhancr II, RF Conductr MC, RF Marinr, RF Marinr 5F SC/ 5F SCXL, 5F SCXS and 5F SCXXL,
Stent, Superficial Femoral Artery
FDA Pre-Market Approval
FDA Class 3
·Innova Vascular Self-Expanding Stent with Delivery System
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·AcrySof IQ ReSTOR Posterior Chamber Intraocular Lenses
Total, Prostate Specific Antigen (Noncomplexed & Complexed) For Detection Of Prostate Cancer
FDA Pre-Market Approval
FDA Class 3
·ARCHITECT Total PSA / Alinity i Total PSA
Ablation Catheter, Renal Denervation
FDA Pre-Market Approval
FDA Class 3
·Symplicity Spyral Multi Electrode Renal Denervation Catheter
Chromogenic In Situ Hybridization, Nucleic Acid Amplification, Her2/Neu Gene, Breast Cancer
FDA Pre-Market Approval
FDA Class 3
·VENTANA HER2 Dual ISH DNA Probe Cocktail
Agent, Absorbable Hemostatic, Collagen Based
FDA Pre-Market Approval
FDA Class 3
·SURGIFLO® Hemostatic Matrix, SURGIFLO® Hemostatic Matrix Kit with Thrombin, SURGIFOAM® Absorbable Gelatin Sponge, U.S.P.
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DYNAGEN ICD, INOGEN ICD, ORIGEN ICD
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·BIOMET ORTHOPAK NON-INVASIVE BONE GROWTH STIMULATOR SYSTEM, BIOMET SPINALPAK NON-INVASIVE SPINE FUSION STIMULATOR SYSTEM
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·COOPERVISION METHAFILCON A SOFT EXTENDED WEAR CONTACT LENSES
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAXIMO II ICD, SECURA ICD, VIRTUOSO II DR/VR ICD
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·ENDOTAK RELIANCE G/SG LEADS
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·GORE EXCLUDER AAA ENDOPROSTHESIS
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·CONSULTA CRT-P, SYNCRA CRT-P, VIVA CRT-P