6 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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Boston Keratoprosthesis, Type I Lucia
FDA 510(k)
FDA Class 2
·Ophthalmic
Keratoprosthesis, Permanent Implant
FDA classification
FDA Class 2
·Keratoprosthesis, Permanent Implant
VIDAS LYME IGG
FDA 510(k)
FDA Class 2
·Microbiology
LATERAL FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
Reagent, Borrelia Serological Reagent
FDA classification
FDA Class 2
·Reagent, Borrelia Serological Reagent
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar