Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ItalyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Revenio GroupLabelled by claude-sonnet-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Centervue with 13 510(k) clearances. The most recent is a 510(k) clearance dated Mar 17, 2025: MAIA (AHMACME001).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Mar 17, 2025 | MAIA (AHMACME001)K243504 · MYC | 510(k) clearances |
| Aug 22, 2024 | iCare ALTIUS CWK234076 · NFJ | 510(k) clearances |
| Dec 21, 2021 | DRSplusK213705 · MYC | 510(k) clearances |
| Aug 19, 2021 | EIDON FA, EIDON, EIDON AF, EIDON UWFLK211328 · MYC | 510(k) clearances |
| Nov 15, 2019 | DRSplusK192113 · MYC | 510(k) clearances |
| Jul 16, 2018 | EIDON FAK180526 · MYC | 510(k) clearances |
| May 30, 2018 | Retia 2K180293 · MYC | 510(k) clearances |
| Jun 8, 2016 | MAIAK153181 · MYC | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
