11 results
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40ms
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Sources: EU EUDAMED, US FDA
Cement Restrictor
FDA registration
HOWMEDICA OSTEONICS CORP·1 product·🇺🇸 United States
UNIVERSAL BONE CEMENT KIT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Cement Obturator
FDA classification
FDA Class 2
·Cement Obturator
V. Mueller
FDA registration
STERIS CORPORATION·1 product·🇺🇸 United States
V. Mueller
FDA registration
STERIS Corporation·1 product·🇺🇸 United States
InterFuse L Intervertebral Body Fusion Device
FDA registration
NEXT ORTHOSURGICAL·1 product·🇺🇸 United States
Spirometer
FDA registration
COVIDIEN·1 product·🇺🇸 United States
APEX ELECTRIC HANDPIECE SYSTEM
FDA 510(k)
FDA Class 1
·Dental
INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
Handpiece, Direct Drive, Ac-Powered
FDA classification
FDA Class 1
·Handpiece, Direct Drive, Ac-Powered
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar