Medcad FDA Approvals

0 new drug approvals and 8 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
MedCAD® AccuStride System510(k)Mar 27, 2026Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Mar 27, 2026
MedCAD® AccuStride System510(k)Nov 4, 2025Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Nov 4, 2025
MedCAD® AccuStride System510(k)Mar 13, 2025Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Mar 13, 2025
MedCAD® AccuPlate® 3DTi Patient-Specific Plating System510(k)Sep 26, 2023Dental	Dental	510(k)Substantially Equivalent (Traditional)	Sep 26, 2023
MedCAD AccuPlan Orthopedics System510(k)Sep 20, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Sep 20, 2023
MedCAD AccuPlan System510(k)Mar 7, 2023Dental	Dental	510(k)Substantially Equivalent (Traditional)	Mar 7, 2023
MedCAD AccuShape Titanium Patient-Specific Cranial Implant510(k)Aug 26, 2022Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Aug 26, 2022
MedCAD® AccuPlate® Patient-Specific Plate510(k)Feb 12, 2021Dental	Dental	510(k)Substantially Equivalent (Traditional)	Feb 12, 2021