1,610 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Wearable Automated External Defibrillator
FDA Pre-Market Approval
FDA Class 3
·LifeVest Wearable Defibrillator
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·GenVisc® 850
Wearable Automated External Defibrillator
FDA Pre-Market Approval
FDA Class 3
·LIFEVEST WEARABLE DEFIBRILLATOR
Wearable Automated External Defibrillator
FDA Pre-Market Approval
FDA Class 3
·LIFEVEST WEARABLE DEFIBRILLATOR
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·prodisc C
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Bellafill Dermal Filler
Wearable Automated External Defibrillator
FDA Pre-Market Approval
FDA Class 3
·LifeVest Wearable Defibrillator Models 4000 and 5100
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Bellafill® Dermal Filler
Tissue Adhesive For Internal Use
FDA Pre-Market Approval
FDA Class 3
·COHERA MEDICAL TISSUGLU
Optical Diagnostic Device For Melanoma Detection
FDA Pre-Market Approval
FDA Class 3
·MELAFIND
Wearable Automated External Defibrillator
FDA Pre-Market Approval
FDA Class 3
·LifeVest Wearable Defibrillator
Generator, Shock-Wave, For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·SIEMENS SONOCUR BASIC SYSTEM
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·SECURE-C CERVICAL ARTIFICIAL DISC
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·Closer Vascular Sealing System (VSS)
Aspiration Therapy System
FDA Pre-Market Approval
FDA Class 3
·Pathway Clinical Trial Cohort
Wearable Automated External Defibrillator
FDA Pre-Market Approval
FDA Class 3
·WEARABLE CARDIOVERTER DEFIBRILLATOR (WCD) 2000 LIFEVEST
Wearable Automated External Defibrillator
FDA Pre-Market Approval
FDA Class 3
·LifeVest Wearable Defibrillator
Wearable Automated External Defibrillator
FDA Pre-Market Approval
FDA Class 3
·LIFEVEST WEARABLE DEFIBRILLATOR
Gases Used Within Eye To Place Pressure On Detached Retina
FDA Pre-Market Approval
FDA Class 3
·PERFLUOROPROPANE FOR PNEUMATIC RETINOPEXY
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·prodisc - C and prodisc - C Nova (Indicated for Single Level Use)