17 results
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41ms
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Sources: EU EUDAMED, US FDA
AXIOM® Second Generation Knee System
FDA registration
MICROPORT ORTHOPEDICS INC.·1 product·🇺🇸 United States
MicroPortOrtho6872 (LN,WH,SP) - AXIOM Second Generation Knee System
FDA registration
ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States
MicroPortOrtho6872 (LN,WH,SP) - AXIOM Second Generation Knee System
FDA registration
Isomedix Operations, Inc.·1 product·🇺🇸 United States
MicroPortOrtho6872 (LN,WH,SP) - AXIOM Second Generation Knee System
FDA registration
ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States
SECOND GENERATION KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Lady-Comp
FDA UDI
Valley Electronics AG·07629999894334·
PainBlocker
FDA registration
Epimed International, Inc.·1 product·🇺🇸 United States
ACU-DISPO-CURETTE
FDA registration
ACUDERM, INC.·1 product·🇺🇸 United States
PainBlocker
FDA registration
EPIMED INTERNATIONAL, INC.·1 product·🇺🇸 United States
ISOMEDIX OPERATIONS INC.
FDA registration
ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States
Isomedix Operations, Inc.
FDA registration
Isomedix Operations, Inc.·1 product·🇺🇸 United States
Arthrex®
FDA UDI
ARTHREX, INC.·00888867052413·AIM GD LT,LOCK DISTAL FIBULA PLT
MEDAID DUAL CHANNEL TENS
FDA 510(k)
FDA Class 2
·Neurology
VIVALITH II 301 PULSE GENERATOR
FDA 510(k)
FDA Class 3
·Cardiovascular
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
FDA classification
FDA Class 2
·Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Implantable Pacemaker Pulse-Generator
FDA classification
FDA Class 3
·Implantable Pacemaker Pulse-Generator
Stimulator, Nerve, Transcutaneous, For Pain Relief
FDA classification
FDA Class 2
·Stimulator, Nerve, Transcutaneous, For Pain Relief