Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled 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 Ovesco Endoscopy with 15 510(k) clearances. The most recent is a 510(k) clearance dated Oct 2, 2026: stentFIX System Set (100.50n).
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 2, 2026 | stentFIX System Set (100.50n)K260487 · PKL | 510(k) clearances |
| Sep 14, 2026 | colonic FTRD Set (200.70); diagnostic FTRD Set (200.76); gastroduodenal FTRD Set (200.72)K253481 · PKL | 510(k) clearances |
| Dec 18, 2025 | OTSCneo System Set (100.03n-14n, 100.27n-31n)K251562 · PKL | 510(k) clearances |
| May 22, 2025 | ArgoCap (200.52)K242586 · OCX | 510(k) clearances |
| Aug 26, 2024 | BARS Set (100.60)K241858 · PKL | 510(k) clearances |
| Aug 11, 2022 | LiftUp (Ref. Nr.: 200.56.01), LiftUp Kit (Ref. Nr.: 200.56.02)K221385 · PLL | 510(k) clearances |
| Jun 2, 2020 | gastroduodenal FTRD SetK200684 · PKL | 510(k) clearances |
| Oct 22, 2019 | stentfix OTSC System SetK183309 · PKL | 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
