647 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·Light Adjustable Lens (LAL) and Light Delivery Device (LDD)
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·RxSight Light Adjustable Lens (LAL), Light Delivery Device (LDD)
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·Light Adjustable Lens (LAL) and Light Delivery Device (LDD)
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·RxSight Light Adjustable Lens (LAL) and Light Delivery Device
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·LIGHT ADJUSTABLE LENS (LAL) AND LIGHT DELIVERY DEVICE (LDD)
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·REPLY & ESPRIT SR & DR Pacemakers
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·RxSight Light Adjustable Lens (LAL) and Light Delivery Device (LDD)
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·RxSight Light Adjustable Lens (LAL) and light Delivery Device (LDD)
Cardiac Ablation Percutaneous Catheter
FDA classification
FDA Class 3
·Cardiac Ablation Percutaneous Catheter
Generator, Shock-Wave, For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·HEALTHTRONICS OSSATRON
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS PRESCRIPTION INSERTS
Generator, Shock-Wave, For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·HEALTHTRONICS OSSATRON
Generator, Shock-Wave, For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·HEALTHTRONICS OSSATRON
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS PRESCRIPTION INSERTS
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC WIKTOR PRIME CORONARY STENT DELIVERY SYSTEM
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS® Corneal Implants
Occluder, Patent Ductus, Arteriosus
FDA Pre-Market Approval
FDA Class 3
·NIT-OCCLUD SYSTEM
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS PRESCRIPTION INSERTS/INTACS CORNEAL IMPLANTS
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS PRESCRIPTION INSERTS
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS CORNEAL RING SEGMENTS