32 results
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46ms
·
Sources: EU EUDAMED, US FDA
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012016·PedFuse Respond, SLD, 7.0mm x 55mm
TRINITY ACETABULAR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SM-EXTRA WIDE (RBM) IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
Oscar PTA
FDA UDI
Biotronik AG·07640130455658·
Oscar
FDA UDI
Biotronik AG·07640130455764·
Oscar PTA
FDA UDI
Biotronik AG·07640130455641·
Oscar
FDA UDI
Biotronik AG·07640130455771·
Oscar
FDA UDI
Biotronik AG·07640130455757·
Oscar PTA
FDA UDI
Biotronik AG·07640130455665·
Wire, Guide, Catheter
FDA classification
FDA Class 2
·Wire, Guide, Catheter
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
FDA classification
FDA Class 2
·Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Implant, Endosseous, Root-Form
FDA classification
FDA Class 2
·Implant, Endosseous, Root-Form