Medimaging Integrated Solution, Inc (Miis) 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
MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus Endoscope Display System -Video Box (EVS 700)510(k)Dec 23, 2025Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Dec 23, 2025
MiiS Horus Bronchoscope; MiiS Horus Endoscope Display System -Tablet; MiiS Horus Endoscope Display System -Video Box510(k)May 1, 2024Ear, Nose, Throat	Ear, Nose, Throat	510(k)Substantially Equivalent (Traditional)	May 1, 2024
VersaVue Single-Use Flexible Cystoscope, VersaVue Tablet, and VersaVue Video Box510(k)Oct 6, 2023Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Oct 6, 2023
ENT Nasopharyngoscope and Accessories510(k)Jul 1, 2022Ear, Nose, Throat	Ear, Nose, Throat	510(k)Substantially Equivalent (Traditional)	Jul 1, 2022