Company ยท IT
Centervue S.P.A.
FDA 510(k) clearances and medical device recalls filed under this name, 2010 to 2025. Name variants (Inc, Corp, punctuation) are merged.
13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Mar 17, 2025 | K243504 | MAIA (AHMACME001) Centervue S.P.A., IT | MYC |
| Aug 22, 2024 | K234076 | iCare ALTIUS CW Centervue S.P.A., IT | NFJ |
| Dec 21, 2021 | K213705 | DRSplus Centervue S.P.A., IT | MYC |
| Aug 19, 2021 | K211328 | EIDON FA, EIDON, EIDON AF, EIDON UWFL Centervue S.P.A., IT | MYC |
| Nov 15, 2019 | K192113 | DRSplus Centervue S.P.A., IT | MYC |
| Jul 16, 2018 | K180526 | EIDON FA Centervue S.P.A., IT | MYC |
| May 30, 2018 | K180293 | Retia 2 Centervue S.P.A., IT | MYC |
| Jun 8, 2016 | K153181 | MAIA Centervue S.P.A., IT | MYC |
| Jun 30, 2015 | K150320 | COMPASS Centervue S.P.A., IT | MYC |
| Nov 12, 2014 | K142047 | EIDON Centervue S.P.A., IT | MYC |
| Apr 23, 2014 | K133758 | CENTERVUE MACULAR INTEGRITY ASSESSMENT Centervue S.P.A., IT | HLI |
| Oct 27, 2010 | K101935 | CENTERVUE DIGITAL RETINOGRAPHY SYSTEM Centervue S.P.A., IT | HKI |
| May 27, 2010 | K092187 | MAIA, MODEL 1 Centervue S.P.A., IT | HPT |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||