980 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Lens, Contact, Orthokeratology, Overnight
FDA Pre-Market Approval
FDA Class 3
·Paragon Z CRT and Paragon Z CRT Dual Axis Rigid Gas Permeable Contact Lenses in Clear and Tints
Lens, Contact (Rigid Gas Permeable), Extended Wear
FDA Pre-Market Approval
FDA Class 3
·Paragon CRT, Paragon CRT 100, Paragon CRT Dual Axis, and Paragon RG-4 Rigid Gas Permeable Contact Lenses in Clear and Ti
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·Akreos Posterior Chamber Intraocular Lens
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·DA+C & DA+T SERIES
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·VITATRON DA+ C SERIES PULSE GENERATORS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·VITATRON DA+C & T SERIES
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·VITATRON DA+ C & T SERIES
Catheter, Coronary, Atherectomy
FDA Pre-Market Approval
FDA Class 3
·Diamondback 360 Coronary Orbital Atherectomy Device (OAD)
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·VITATRON DA+ C & T SERIES IPGS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·DA+ C-SERIES AND DA+ T-SERIES
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·DA+ C-SERIES & DA+ T-SERIES
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·DA+C SERIES & DA+T SERIES
Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold, Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE
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
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·VITATRON DA+C-SERIES/VITATRON DA+T SERIES
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·VITATRON DA + C-SERIESAND VITATRON DA + T-SERIES
Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System
FDA Pre-Market Approval
FDA Class 3
·FoundationOne Liquid CDx (F1LCDx)
Generator, Shock-Wave, For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·HEALTHTRONICS OSSATRON
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS PRESCRIPTION INSERTS
Generator, Shock-Wave, For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·HEALTHTRONICS OSSATRON