813 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·NIDEK EC-5000 EXCIMER LASER SYSTEM
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·NIDEK EC-5000 EXCIMER LASER SYSTEM
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·NIDEK EXCIMER LASER SYSTEM EC-5000
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·NIDEK EC-5000 EXCIMER LASER SYSTEM
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·NIDEK EC-5000 EXCIMER LASER SYSTEM
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·NIDEK EC-5000 EXCIMER LASER SYSTEM
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·EC-5000 EXCIMER LASER SYSTEM
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·NIDEK EC-5000 EXCIMER LASER SYSTEM
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·NIDEK EC-5000 EXCIMER LASER
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·EC-5000 EXCIMER LASER SYSTEM
TRANSDUCER FOR KONTROL 5MHZ SIGMA 20
FDA 510(k)
FDA Class 3
·Unknown
Sensor, Glucose, Invasive
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC MINIMED CONTINUOUS SUBCUTANEOUS GLUCOSE MONITORING SYSTEM
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·CARPENTIER-EDWARDS DURAFLEX LOW PRESSURE MITRAL BIOPROSTHESIS WITH EXTENDED SUTURE RING, CARPENTIER-EDWARDS DURAFLEX LO
Aortic Valve, Prosthesis, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·COREVALVE EVOLUT BIOPROSTHESIS, CORE VALVE BIOPROSTHESIS, ACCUTRAK DELIVERY CATHETER SYSTEM, GEN 3 & GEN4 COMPRESSION LO
Aortic Valve, Prosthesis, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·EnVeo PRO Delivery Catheter System, EnVeo R Delivery Catheter System, Evolut PRO+ Delivery Catheter System, EnVeo PRO Lo
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·RADIESSE INJECTABLE IMPLANT FOR SUB-DERMAL IMPLANTATION FOR RESTORARION AND OR/ CORRECTION OF THE SIGNS OF FACIAL FAT LO
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·RADIESSE INJECTABLE IMPLANT FOR SUB-DERMAL IMPLANTATION FOR RESTORATION AND OR CORRECTION FOR THE SIGNS OF FACIAL FAT LO
Cancer-Related Germline Gene Mutation Detection System
FDA Pre-Market Approval
FDA Class 3
·myChoice HRD CDx
Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System
FDA Pre-Market Approval
FDA Class 3
·myChoice CDx
Atrial Defibrillator
FDA classification
FDA Class 3
·Atrial Defibrillator