10,000 results
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66ms
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Sources: EU EUDAMED, US FDA
Rongeur, Powered
FDA classification
FDA Class 2
·Rongeur, Powered
Stimulator, Autonomic Nerve, Implanted (Depression)
FDA classification
FDA Class 3
·Stimulator, Autonomic Nerve, Implanted (Depression)
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·VISTA LORDOTIC INTERBODY FUSION CAGE
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VITALITY AVT AND THE PROGRAMMER SOFTWARE APPLICATION MODEL 2812
Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK INTERBODY FUSION SYSTEM, BP/LORDOTIC DEVICE
Separator, Automated, Blood Cell And Plasma, Therapeutic
FDA Pre-Market Approval
FDA Unclassified
·PROSORBA COLUMN
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VENTAK VITALITY AVT AICD, MODELS A135 AND A155, MODEL 2920 PROGRAMMER WITH MODEL 2812 APPLICATION SOFTWARE VERSION 1.2
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·LT-CAGE LUMBAR TAPERED FUSION DEVICE
Filler, Bone Void, Synthetic Peptide
FDA Pre-Market Approval
FDA Class 3
·PearlMatrix Bone Graft
Access Thyroglobulin
FDA UDI
Beckman Coulter, Inc.·15099590754501·Access Thyroglobulin assay is a paramagnetic pa...
Test, Volatile Organic Compounds Breath Analysis
FDA classification
Test, Volatile Organic Compounds Breath Analysis
Acute Coronary Syndrome Event Detector
FDA Pre-Market Approval
FDA Class 3
·Guardian System
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·LT-CAGE TAPERED FUSION DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK VISTA INTERBODY FUSION DEVICE
Assay, Enzyme Linked Immunosorbent, Hepatitis C Virus
FDA Pre-Market Approval
FDA Class 2
·HOME ACCESS HEPATITIS C CHECK
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·LORDOTEC(TM) TAPERED FUSION DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK VISTA INTERBODY FUSION CAGE
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·ADVISA SR MRI
Dorsal Root Ganglion Stimulator For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Axium Neurostimulator System