Double Medical Technology, Inc. FDA Approvals

0 new drug approvals and 9 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
Universal Spinal System510(k)Nov 18, 2025Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Nov 18, 2025
Locking Screw,CoCrMo510(k)Dec 4, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Abbreviated)	Dec 4, 2024
Posterior Cervical Spine System510(k)Nov 22, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Nov 22, 2023
Cervical Plate System510(k)Mar 14, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Mar 14, 2023
Advanced Bone Plate510(k)Jan 25, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Jan 25, 2023
Anatomic Bone Plate510(k)Jan 18, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Jan 18, 2023
Metal Cannulated Screw510(k)Jan 10, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Jan 10, 2023
Advanced Intramedullary Nail System510(k)Dec 21, 2022Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Dec 21, 2022
Metal Bone Screw510(k)Dec 12, 2022Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Dec 12, 2022