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 its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Neptune Medical with 7 510(k) clearances. The most recent is a 510(k) clearance dated Sep 18, 2026: Pathfinder Endoscope Overtube.
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.
| Sep 18, 2026 | Pathfinder Endoscope OvertubeK262262 · FED | 510(k) clearances |
| Sep 3, 2026 | Triton 1 SystemK260503 · FDF | 510(k) clearances |
| Jun 27, 2024 | Pathfinder® CR SystemK240853 · FED | 510(k) clearances |
| Jul 28, 2023 | Pathfinder Endoscope Overtube with Balloon DeviceK230801 · FED | 510(k) clearances |
| May 28, 2021 | Pathfinder Endoscope OvertubeK211301 · FED | 510(k) clearances |
| May 25, 2021 | Pathfinder Endoscope CapK210915 · FDS | 510(k) clearances |
| Aug 30, 2019 | Pathfinder Endoscope OvertubeK191415 · FED | 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
