Medcad

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251709MedCAD® AccuStride™ SystemNovember 4, 2025
K241811MedCAD® AccuStride™ SystemMarch 13, 2025
K230398MedCAD® AccuPlate® 3DTi Patient-Specific Plating SystemSeptember 26, 2023
K223421MedCAD AccuPlan Orthopedics SystemSeptember 20, 2023
K223024MedCAD AccuPlan SystemMarch 7, 2023
K220357MedCAD AccuShape Titanium Patient-Specific Cranial ImplantAugust 26, 2022
K193280MedCAD® AccuPlate® Patient-Specific PlateFebruary 12, 2021
K192282MedCAD® AccuPlan® SystemOctober 29, 2020