6 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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LumiVy Lumbar IBF System
FDA 510(k)
FDA Class 2
·Orthopedic
MOBILE MIM
FDA 510(k)
FDA Class 2
·Radiology
ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A)
FDA 510(k)
FDA Class 2
·Ophthalmic
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Lenses, Soft Contact, Daily Wear
FDA classification
FDA Class 2
·Lenses, Soft Contact, Daily Wear
System, Image Processing, Radiological
FDA classification
FDA Class 2
·System, Image Processing, Radiological