32 results
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48ms
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Sources: EU EUDAMED, US FDA
Phadia 250 and Phadia 2500, Phadia 5000 Instrument E series
FDA registration
PHADIA GMBH·1 product·🇩🇪 Germany
LimFlow ARC
FDA registration
Nitinol Devices & Components Costa Rica, S. R. L.·1 product·🇨🇷 Costa Rica
Phadia 250 and Phadia 2500, Phadia 5000 Instrument E series
FDA registration
PHADIA AB·1 product·🇸🇪 Sweden
Phadia 250 and Phadia 2500, Phadia 5000 Instrument E series
FDA registration
PHADIA AB·1 product·🇸🇪 Sweden
Synergy Health AST, SRL
FDA registration
Synergy Health AST, SRL·1 product·🇨🇷 Costa Rica
Barrigel
FDA registration
Q-MED AB·1 product·🇸🇪 Sweden
Barrigel
FDA registration
R.K. Manufacturing·1 product·🇺🇸 United States
Hive Stand-alone Anterior Lumbar Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
AGILITY ANKLE REVISION PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
Polymer Patient Examination Glove
FDA classification
FDA Class 1
·Polymer Patient Examination Glove
Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer
FDA classification
FDA Class 2
·Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer
Intervertebral Fusion Device With Integrated Fixation, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Integrated Fixation, Lumbar