26 results
·
44ms
·
Sources: EU EUDAMED, US FDA
Arthrosurface® Total Toe - Proximal Phalanx Implant
FDA registration
ARTHROSURFACE, INC.·1 product·🇺🇸 United States
MODIFICATION TO SPACE CPSXL BONE CEMENT
FDA 510(k)
FDA Class 2
·Orthopedic
POWERHEART AED G3 SEMI-AUTOMATIC, POWERHEART AED G3 AUTOMATIC, POWERHEART AED G3 PRO, POWERHEART AED G3 PLUS
FDA 510(k)
FDA Class 3
·Cardiovascular
Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
FDA classification
FDA Class 2
·Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Cement, Bone, Vertebroplasty
FDA classification
FDA Class 2
·Cement, Bone, Vertebroplasty
Automated External Defibrillators (Non-Wearable)
FDA classification
FDA Class 3
·Automated External Defibrillators (Non-Wearable)