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 Palliare, Ltd. with 6 510(k) clearances. The most recent is a 510(k) clearance dated May 2, 2024: EVA15 insufflator.
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 |
|---|---|---|
| May 2, 2024 | EVA15 insufflatorK232902 · HIF | 510(k) clearances |
| Mar 24, 2023 | EVA5 InsufflatorK230474 · FCX | 510(k) clearances |
| Jan 27, 2023 | EVA15 insufflatorK222901 · HIF | 510(k) clearances |
| Jul 8, 2021 | END 200 Endoscopic TubesetK202922 · FCX | 510(k) clearances |
| Oct 21, 2020 | EVA15K202799 · HIF | 510(k) clearances |
| Jul 23, 2020 | EVA 15 InsufflatorK193520 · HIF | 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
