Data / Medical devices / Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula / United States
FDA-registered makers of Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula in the United States: 6 establishments
6 establishments in the United States are registered with the FDA to make Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula (product code ODD). 6 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula
- Product code
- ODD
- Country
- United States
Makers of Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Conmed Corporation | Utica, NY, United States | Complaint file establishment, Manufacturer | 2 | April 27, 1995 | 0 | 0 | 0 | api.fda.gov |
| United States Endoscopy Group, Inc. | Mentor, OH, United States | Complaint file establishment, Manufacturer | 2 | November 6, 2020 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Marlborough, MA, United States | Complaint file establishment, Specification developer | 1 | November 28, 1983 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Coventry, RI, United States | Manufacturer | 1 | November 28, 1983 | 0 | 0 | 0 | api.fda.gov |
| Conmed Corporation | Westborough, MA, United States | Specification developer | 1 | April 9, 1982 | 0 | 0 | 0 | api.fda.gov |
| Wilson-Cook Medical Inc. | Winston Salem, NC, United States | Complaint file establishment, Manufacturer | 1 | March 20, 2018 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.