Medical Device Manufacturer · IT , Padova

Centervue S.P.A. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2010

13

Total

13

Cleared

0

Denied

FDA 510(k) cleared devices by Centervue S.P.A. Ophthalmic ✕

13 devices

1-12 of 13

Cleared Mar 17, 2025

MAIA (AHMACME001)

Ophthalmic · 125d

Cleared Aug 22, 2024

iCare ALTIUS CW

Ophthalmic · 245d

Cleared Dec 21, 2021

Ophthalmic · 27d

Cleared Aug 19, 2021

EIDON FA, EIDON, EIDON AF, EIDON UWFL

Ophthalmic · 108d

Cleared Nov 15, 2019

Ophthalmic · 102d

Cleared Jul 16, 2018

Ophthalmic · 139d

Cleared May 30, 2018

Ophthalmic · 118d

Cleared Jun 08, 2016

Ophthalmic · 218d

Cleared Jun 30, 2015

Ophthalmic · 141d

Cleared Nov 12, 2014

Ophthalmic · 107d

Cleared Apr 23, 2014

CENTERVUE MACULAR INTEGRITY ASSESSMENT

Ophthalmic · 133d

Cleared Oct 27, 2010

CENTERVUE DIGITAL RETINOGRAPHY SYSTEM

Ophthalmic · 107d