Dio Medical Corporation FDA Approvals

0 new drug approvals and 4 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
Rexious Spinal Fixation System510(k)Oct 25, 2022Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Oct 25, 2022
FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate System, and BALTEUM & BALTEUM-ONE Lumbar Plate System510(k)Oct 18, 2022Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Oct 18, 2022
UNITY Sacroiliac Joint Fixation System510(k)Oct 13, 2022Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Oct 13, 2022
FaSet Fixation System510(k)Oct 5, 2022	—	510(k)Substantially Equivalent (Traditional)	Oct 5, 2022