4,842 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·ORTHOPAK(R) BONE GROWTH STIMULATOR
Stimulator, Invasive Bone Growth
FDA Pre-Market Approval
FDA Class 3
·OSTEOSTIM(TM) IMPLANTABLE BONE GROWTH STIMULATOR
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·Biomet OrthoPak Non-invasive Bone Growth Stimulator System and Biomet SpinalPak Non-invasive Spine Fusion Stimulator Sys
Stimulator, Invasive Bone Growth
FDA Pre-Market Approval
FDA Class 3
·EBI OSTEOGEN IMPLANTABLE BONE GROWTH STIMULATORS
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·Biomet® OrthoPak Non-invasive Bone Growth Stimulator System
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·EBI BONE HEALING SYSTEM MODEL 1020
Stimulator, Invasive Bone Growth
FDA Pre-Market Approval
FDA Class 3
·EBI OsteoGen Impantable Bone Growth Stimulators
Stimulator, Invasive Bone Growth
FDA Pre-Market Approval
FDA Class 3
·OSTEOGEN IMPLANTABLE SPINAL FUSION STIMULATOR
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·Biomet® OrthoPak® Non-invasive Bone Growth Stimulator System & Biomet® SpinalPak® Non-invasive Spine Fusion Stimulator S
Stimulator, Invasive Bone Growth
FDA Pre-Market Approval
FDA Class 3
·OSTEOSTIM(R)
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·EBI BONE HEALING SYSTEM(R)-MODEL 1026
Stimulator, Invasive Bone Growth
FDA Pre-Market Approval
FDA Class 3
·EBI OSTEOGEN IMPLANTABLE BONE GROWTH STIMULATOR
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·THE BIOMET ORTHOPAK NON-INVASIVE BONE GROWTH STIMULATOR SYSTEM, THE BIOMET SPINALPAK NON-INVASIVE SPINE FUSION STIMULATO
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·Biomet® OrthoPak® Non-invasive Bone Growth Stimulator System and Biomet® SpinalPak® Non-invasive Spine Fusion Stimulator
Lens, Contact (Rigid Gas Permeable), Extended Wear
FDA classification
FDA Class 3
·Lens, Contact (Rigid Gas Permeable), Extended Wear
Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia
FDA Pre-Market Approval
FDA Class 3
·MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear
Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia
FDA Pre-Market Approval
FDA Class 3
·MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear
Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia
FDA Pre-Market Approval
FDA Class 3
·MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear
Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia
FDA Pre-Market Approval
FDA Class 3
·MiSight 1 Day (omafilcon A)
Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia
FDA Pre-Market Approval
FDA Class 3
·MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear