Centervue S.P.A. 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
MAIA (AHMACME001)510(k)Mar 17, 2025Ophthalmic	Ophthalmic	510(k)Substantially Equivalent (Traditional)	Mar 17, 2025
iCare ALTIUS CW510(k)Aug 22, 2024Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Aug 22, 2024
DRSplus510(k)Dec 21, 2021Ophthalmic	Ophthalmic	510(k)Substantially Equivalent (Special)	Dec 21, 2021
EIDON FA, EIDON, EIDON AF, EIDON UWFL510(k)Aug 19, 2021Ophthalmic	Ophthalmic	510(k)Substantially Equivalent (Special)	Aug 19, 2021