10 results
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41ms
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Sources: EU EUDAMED, US FDA
Kwik-Fix/TS Cervical System
FDA registration
SOUTHERN SPINE, LLC·1 product·🇺🇸 United States
SOUTHERN SPINE ANTERIOR CERVICAL STABILIZATION SYSTEM, KWIK- FIX CERVICAL SYSTEM, AND KWIK-FIX / TS CERVICAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Access II
FDA registration
CANUTE INTERNATIONAL MEDICAL SERVICES (CANADA) INC·6 products·🇨🇦 Canada
Scaler Ultrasonic Device
FDA registration
SATELEC-ACTEON GROUP·1 product·🇫🇷 France
UniCel DxI 800 Access Immunoassay System (P/N: 973100)
FDA registration
BECKMAN COULTER, INC.·6 products·🇺🇸 United States
MODIFICATION TO EBI SPINELINK SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
IMMIX BONE GRAFT EXTENDER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Appliance, Fixation, Spinal Intervertebral Body
FDA classification
FDA Class 2
·Appliance, Fixation, Spinal Intervertebral Body
Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction
FDA classification
FDA Class 2
·Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction
Orthosis, Spondylolisthesis Spinal Fixation
FDA classification
FDA Class 2
·Orthosis, Spondylolisthesis Spinal Fixation