Centervue S.P.A.
Centervue S.P.A. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2025.
Top product codes for Centervue S.P.A.
Recent clearances by Centervue S.P.A.
- K243504 — MAIA (AHMACME001)
- K234076 — iCare ALTIUS CW
- K213705 — DRSplus
- K211328 — EIDON FA, EIDON, EIDON AF, EIDON UWFL
- K192113 — DRSplus
- K180526 — EIDON FA
- K180293 — Retia 2
- K153181 — MAIA
- K150320 — COMPASS
- K142047 — EIDON
- K133758 — CENTERVUE MACULAR INTEGRITY ASSESSMENT
- K101935 — CENTERVUE DIGITAL RETINOGRAPHY SYSTEM
- K092187 — MAIA, MODEL 1
Data sourced from openFDA. This site is unofficial and independent of the FDA.