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Centervue S.P.A.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243504MAIA (AHMACME001)March 17, 2025
K234076iCare ALTIUS CWAugust 22, 2024
K213705DRSplusDecember 21, 2021
K211328EIDON FA, EIDON, EIDON AF, EIDON UWFLAugust 19, 2021
K192113DRSplusNovember 15, 2019
K180526EIDON FAJuly 16, 2018
K180293Retia 2May 30, 2018
K153181MAIAJune 8, 2016
K150320COMPASSJune 30, 2015
K142047EIDONNovember 12, 2014
K133758CENTERVUE MACULAR INTEGRITY ASSESSMENTApril 23, 2014
K101935CENTERVUE DIGITAL RETINOGRAPHY SYSTEMOctober 27, 2010
K092187MAIA, MODEL 1May 27, 2010