Ortho Development Corp. FDA Approvals

0 new drug approvals and 5 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
Balanced Knee System TriMax Porous Femoral Components510(k)Dec 19, 2025Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Dec 19, 2025
Trivicta® Hip Stem510(k)May 22, 2025Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	May 22, 2025
BKS Revision System510(k)Oct 25, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Special)	Oct 25, 2024
Legend® Acetabular Shell510(k)Oct 11, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Special)	Oct 11, 2024
Trivicta Hip Stem510(k)Mar 8, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Mar 8, 2024