Medical device makerLabelled by claude-haiku-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 13, 2026, FDA's public records list Prexion Corporation with 9 510(k) clearances. The most recent is a 510(k) clearance dated Sep 8, 2023: PreXion3D Expedition.
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 |
|---|---|---|
| Sep 8, 2023 | PreXion3D ExpeditionK232166 · OAS | 510(k) clearances |
| Jan 12, 2023 | PreXion3D ExpeditionK222150 · OAS | 510(k) clearances |
| Jul 22, 2022 | PreXion3D Explorer PROK221525 · OAS | 510(k) clearances |
| Feb 23, 2021 | PreXion3D Explorer PROK203784 · OAS | 510(k) clearances |
| Apr 9, 2020 | PreXion3D Explorer EXK193329 · OAS | 510(k) clearances |
| Apr 15, 2019 | PreXion3D ExplorerK190320 · OAS | 510(k) clearances |
| Aug 17, 2018 | PreXion 3D ExcelsiorK181983 · OAS | 510(k) clearances |
| Jan 19, 2018 | PreXion3D ExcelsiorK173878 · OAS | 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
