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., part of Cook MedicalLabelled 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 Cook Endoscopy with 4 510(k) clearances. The most recent is a 510(k) clearance dated Mar 5, 2020: Instinct Plus Endoscopic Clipping Device.
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 |
|---|---|---|
| Mar 5, 2020 | Instinct Plus Endoscopic Clipping DeviceK192697 · PKL | 510(k) clearances |
| Sep 25, 2009 | HERCULES 3 STAGE WIRE GUIDED DILATION BALLOONK090183 · KNQ | 510(k) clearances |
| Feb 6, 2009 | ECHOTIP ULTRA ULTRASOUND NEEDLEK083330 · FCG | 510(k) clearances |
| Dec 1, 2006 | COOK ENDOSCOPY ESOPHAGEAL DILATION BALLOONK061937 · KNQ | 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
