10,000 results
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35ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Implanted Electrical Device Intended For Treatment Of Fecal Incontinence
FDA Pre-Market Approval
FDA Class 3
·Axonics Sacral Neuromodulation (SNM) System for Bowel Control
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·UROLOGIX TARGIS SYSTEM FOR THE TREATMENT OF BPH
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·VIFILCON A SOFT CONTACT LENSES FOR EXTENDED WEAR
Stimulator, Electrical, Implantable, For Incontinence
FDA Pre-Market Approval
FDA Class 3
·Axonics Sacral Neuromodulation (SNM) System for Bowel Control
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·UROLOGIX TARGIS SYSTEM FOR THE TREATMENT OF BPH
Implanted Electrical Device Intended For Treatment Of Fecal Incontinence
FDA Pre-Market Approval
FDA Class 3
·Axonics Sacral Neuromodulation (SNM) System for Urinary Control
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·UROLOGIX TARGIS SYSTEM FOR THE TREATMENT OF BPH
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·IF4 BOARD FOR THE DUAL PROCESSOR INTERFACE SYSTEM
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·VISTAKON (SENOFILCON A) CONTACT LENSES FOR EXTENDED WEAR
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
FDA Pre-Market Approval
FDA Class 3
·Interface Cable for Multi-Electrode Ablation Catheters (nMARQ)
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·UROLOGIX TARGIS SYSTEM FOR THE TREATMENT OF BPH
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLES 22 CHANNEL COCHLEAR IMPLANT SYSTEM FOR CHIL
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·VIFILCON A SOFT CONTACT LENSES FOR EXTENDED WEAR
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX
Tissue Graft Of 6mm And Greater
FDA Pre-Market Approval
FDA Class 3
·DARDIK BIOGRAFT FOR USE IN PERIPHERAL VASCULAR SUR
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Totally Implanted Spinal Cord Stimulator for Pain Relief
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·UROLOGIX TARGIS SYSTEM FOR THE TREATMENT OF BPH
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MODEL 3038 FUNCTION PACT FOR ASP-II 3003 PROGRAMME
Implanted Electrical Device Intended For Treatment Of Fecal Incontinence
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC INTERSTIM SACRAL NERVE STIMULATION THERAPY SYSTEM FOR BOWEL
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·BIOFINITY (COMFILCON A) SOFT CONTACT LENS FOR EXTEND WEAR