5,527 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·NEW VUES (TM)(VIFILCON A)(HYDROPHILIC)SOFT LENSES
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·NEW VUES (TM)(VIFILCON A)(HYDROPHILIC)SOFT LENSES
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·NEW VUES (TM)(VIFILCON A)(HYDROPHILIC)SOFT LENSES
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid® Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid® Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Anular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Anular Closure Device (ACD)
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid® Annular Closure Device - Model Number BAR-A8-8MM (2730815-A&), Barricaid® Annular Closure Device - Model Numb
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·BARRICAID ANULAR CLOSURE DEVICE (ACD)
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Anular Closure Device
NEW ADHESIVE, PELLETHAN ON POLYURETHANE LEADS-MODI
FDA 510(k)
FDA Class 3
·Cardiovascular
Heart-Valve, Mechanical
FDA Pre-Market Approval
FDA Class 3
·MECHANICAL HEART VALVE SJM(R) MASTER SERIES (EXPANDED SEWING CUFF)
System, Test, Her-2/Neu, Ihc
FDA Pre-Market Approval
FDA Class 3
·PATHWAY ANTI-HER-2/NEW (4B5)RABBIT MONOCLONAL PRIMARY ANTIBODY
Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing
FDA Pre-Market Approval
FDA Class 3
·CONSERVE PLUS HIP RESURFACING SYSTEM NEW ENROLLMENT STUDY (NES) PROTOCOL
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·TARGIS TARGETED TRANSURETHRAL THERMOABLATION SYSTEM (TARGIS SYSTEM): NEW POUCH SEALER
VS-1 SILICONE IMPLANT LEADS (NEW SERIAL # TUBE)
FDA 510(k)
FDA Class 3
·Cardiovascular
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·ONE-PIECE ANTERIOR CHAMBER INTRAOCULAR LENSES MODEL 121UV NEW LENS CARRIER
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·ONE-PIECE ANTERIOR CHAMBER INTRAOCULAR LENSES MODEL 121UV NEW LENS CARRIER