6 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
×
CoreLink® M3 Stand-Alone Anterior Lumbar System
FDA 510(k)
FDA Class 2
·Orthopedic
Intervertebral Fusion Device With Integrated Fixation, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Integrated Fixation, Lumbar
AMBIT TUNNELER
FDA 510(k)
FDA Class 2
·Anesthesiology
VOCO PROFLUORID VARNISH
FDA 510(k)
FDA Class 2
·Dental
Catheter, Conduction, Anesthetic
FDA classification
FDA Class 2
·Catheter, Conduction, Anesthetic
Varnish, Cavity
FDA classification
FDA Class 2
·Varnish, Cavity