Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 6 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Riverain Technologies with 5 510(k) clearances and 4 AI-enabled devices. The most recent is a 510(k) clearance dated Dec 3, 2024: ClearRead CT CAC.
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.
| Date | Record | Source |
|---|---|---|
| Dec 3, 2024 | ClearRead CT CACK242188 · JAK | 510(k) clearances |
| Dec 3, 2024 | ClearRead CT CACK242188 · Radiology | AI-enabled devices |
| Dec 5, 2022 | ClearRead CTK221612 · OEB | 510(k) clearances |
| Mar 10, 2022 | ClearRead Xray PneumothoraxK213566 · QFM | 510(k) clearances |
| Mar 10, 2022 | ClearRead Xray PneumothoraxK213566 · Radiology | AI-enabled devices |
| Sep 9, 2016 | ClearRead CTK161201 · OEB | 510(k) clearances |
| Sep 9, 2016 | ClearRead CTK161201 · Radiology | AI-enabled devices |
| Dec 27, 2012 | CLEARREAD +CONFIRMK123526 · LLZ | 510(k) clearances |
| Dec 27, 2012 | CLEARREAD +CONFIRMK123526 · Radiology | AI-enabled devices |
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
