17 results
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41ms
·
Sources: EU EUDAMED, US FDA
Sherlock Abutment
FDA registration
OPEN IMPLANTS·1 product·🇺🇸 United States
Sherlock
FDA registration
Selser Dental Lab., Inc.·1 product·🇺🇸 United States
OPEN IMPLANTS
FDA registration
AVINENT IMPLANT SYSTEM S.L.U.·1 product·🇪🇸 Spain
Sherlock
FDA 510(k)
FDA Class 2
·Dental
StimRouter Neuromodulation System
FDA registration
BIOVENTUS LLC·1 product·🇺🇸 United States
Keratome Blade
FDA registration
Microspecialties LLC·1 product·🇺🇸 United States
StimRouter Neuromodulation System
FDA registration
Bioventus LLC·1 product·🇺🇸 United States
VEO® Lateral Interbody Fusion System
FDA UDI
Choice Spine, LP·00840996134330·LATERAL,CURETTE,STRAIGHT CUP
Materialise Shoulder System
FDA registration
MATERIALISE N.V.·3 products·🇧🇪 Belgium
NEUWAVE Microwave Ablation
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
MSTD0020
FDA registration
ORCHID UNIQUE·1 product·🇺🇸 United States
Materialise Shoulder System
FDA registration
Materialise USA, LLC.·3 products·🇺🇸 United States
StimRouter Neuromodulation System
FDA 510(k)
FDA Class 2
·Neurology
KERATOME BLADE 200200 & 600600
FDA 510(k)
FDA Class 1
·Ophthalmic
Abutment, Implant, Dental, Endosseous
FDA classification
FDA Class 2
·Abutment, Implant, Dental, Endosseous
Stimulator, Peripheral Nerve, Implanted (Pain Relief)
FDA classification
FDA Class 2
·Stimulator, Peripheral Nerve, Implanted (Pain Relief)
Keratome, Ac-Powered
FDA classification
FDA Class 1
·Keratome, Ac-Powered