26 results
·
41ms
·
Sources: EU EUDAMED, US FDA
XN CHECK BF
FDA registration
SYSMEX CORPORATION TECHNO PARK·1 product·🇯🇵 Japan
Claris CBCT
FDA registration
iCRco Inc.·1 product·🇺🇸 United States
ATLAS SPINE PIVOTING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PADPRO, MODEL 2502
FDA 510(k)
FDA Class 3
·Cardiovascular
Automated External Defibrillators (Non-Wearable)
FDA classification
FDA Class 3
·Automated External Defibrillators (Non-Wearable)
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar