347 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Revanesse Versa, Revanesse Versa+ (with lidocaine), Revanesse Lips+ (with lidocaine)
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Revanesse Lips+ with Lidocaine 1.2 mL
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Revanesse Versa 1.0 mL, Revanesse Versa 1.2 mL, Revanesse Versa + with Lidocaine 1.0 mL, Revanesse Versa + with Lidocain
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Revanesse Versa; Revanesse Versa+ with Lidocaine, Revanesse Versa+ with Lidocaine 1.2 mL, Revanesse® Versa 1.2 mL, Reva
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Revanesse Versa+
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Revanesse Versa+
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Revanesse Versa
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Revanesse Versa and Revanesse Versa+
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Revanesse Versa, Revanesse Versa+ with Lidocaine, Revanesse Versa 1.2 mL, Revanesse Versa+ with Lidocaine 1.2 mL, Revane
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·REVANESSE ULTRA
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Revanesse Versa +
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Revanesse Ultra (Revanesse Versa)
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Revanesse Versa, Revanesse Versa+, Revanesse Lips+
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·EON MINI IPG NEUROSTIMULATION SYSTEM
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·GENESIS AND EON FAMILY NEUROSTIMULATION (IPG) SYSTEMS
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·GENESIS NEUROSTIMULATION (IPG) SYSTEM
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·COFLEX® INTERLAMINAR TECHNOLOGY
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·GENESIS NEUROSTIMULATION (IPG) SYSTEM
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·X-STOP INTERSPINOUS SPACER SYSTEM
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·GORE EXCLUDER AAA ENDOPROSTHESIS