926 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·Light Adjustable Lens, Light Delivery Device
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·Light Adjustable Lens and Light Delivery Device
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·Light Adjustable Lens, Light Delivery Device
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·RxSight Light Adjustable Lens and Light Delivery Device
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·Light Adjustable Lens, Light Delivery System
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·RxSight Light Adjustable Lens and Light Delivery Device
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·Light Adjustable Lens, Light Delivery Device
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·RxSight Light Adjustable Lens and Light Delivery System
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·RxSight Light Adjustable Lens and Light Delivery Device
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·RxSight Light Adjustable Lens: Ligh Delivery Device
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·Light Adjustable Lens, Light Delivery Device
Wearable Automated External Defibrillator
FDA Pre-Market Approval
FDA Class 3
·LIFEVEST WEARABLE DEFIBRILLATOR
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS 24 COCHLEAR IMPLANT SYSTEM
Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA Pre-Market Approval
FDA Class 3
·NATURAL-KNEE(R) AND NATURAL KNEE(R)II W/CSTI(TM)
Device, Thermal Ablation, Endometrial
FDA Pre-Market Approval
FDA Class 3
·Cerene Cryotherapy Device
Intravascular Radiation Delivery System
FDA Pre-Market Approval
FDA Class 3
·GALILEO/INTRAVASCULAR RADIOTHERPY SYSTEM
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·EXTERNAL PULSE GENERATOR
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·VARIOUS FAMILIES OF PACEMAKERS
Pulse-Generator, Single Chamber, Sensor Driven, Implantable
FDA Pre-Market Approval
FDA Class 3
·PREVAIL
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·LEGEND PLUS FAMILY OF PACEMAKERS