1,108 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Implant, Auditory Brainstem
FDA Pre-Market Approval
FDA Class 3
·Nucleus® Auditory Brainstem Implant System
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·CVX-300/CVX300-P EXCIMER LASER SYSTEM
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CORDIS SEQUICOR THETA MODELS 233D & 233E
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS CI522 COCHLEAR IMPLANT SYSTEM
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·GUARDIAN(R) ATP II IMPLANTABLE CARDIOVERTER/DIFIB.
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS COCHLEAR IMPLANT SYSTEM
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·SPECTRANETICS EXCIMER LASER
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS 24 AUDITORY BRAINSTEM IMPLANT (ABI)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CORDIS SEQUICOR THETA MODELS 233D & 233E
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Mobi-C Cervical Disc Prosthesis for use at One or Two Levels
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·Nucleus® 24 Cochlear Implant System
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·GEMINI(R) THETA MODEL 415A CARDIAC PACER
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·EXCIMER LASER
Cochlear Implant With Combined Electrical Stimulation And Acoustic Amplification
FDA Pre-Market Approval
FDA Class 3
·Nucleus Hybrid L24 Implant System
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS 24 COCHLEAR IMPLANT SYSTEM
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·Nucleus 24 Cochlear Implant System
Filler, Bone Void, Synthetic Peptide
FDA Pre-Market Approval
FDA Class 3
·i-FACTOR Peptide Enhanced Bone Graft
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·MOBI-C CERVICAL DISC PROSTHESIS (ONE-LEVEL INDICATION)
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·LDR Spine Mobi-C Cervical Disc Prosthesis
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CORDIS SEQUICOR THETA MODELS 233D & 233E