Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in FranceLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Therenva SAS with 5 510(k) clearances and 2 AI-enabled devices. The most recent is a 510(k) clearance dated Oct 25, 2022: EndoNaut.
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 |
|---|---|---|
| Oct 25, 2022 | EndoNautK222070 · OWB | 510(k) clearances |
| Oct 25, 2022 | EndoNautK222070 · Radiology | AI-enabled devices |
| Aug 31, 2021 | EndoNautK212383 · OWB | 510(k) clearances |
| Aug 31, 2021 | EndoNautK212383 · Radiology | AI-enabled devices |
| Sep 21, 2017 | EndoNautK171829 · OWB | 510(k) clearances |
| Apr 12, 2016 | EndoSizeK160376 · LLZ | 510(k) clearances |
| Jul 31, 2014 | ENDOSIZEK141475 · LLZ | 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
