Data / Medical devices / Esophagoscope (Flexible Or Rigid) / United States
FDA-registered makers of Esophagoscope (Flexible Or Rigid) in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Esophagoscope (Flexible Or Rigid) (product code EOX). 7 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Esophagoscope (Flexible Or Rigid)
- Product code
- EOX
- Country
- United States
Makers of Esophagoscope (Flexible Or Rigid) in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Karl Storz Endoscopy-America, Inc. | Auburn, MA, United States | Contract manufacturer, Repackager or relabeler | 7 | January 24, 2020 | 0 | 0 | 0 | api.fda.gov |
| Medtronic Xomed, Inc. | Jacksonville, FL, United States | Manufacturer | 3 | August 29, 2007 | 0 | 0 | 0 | api.fda.gov |
| Cogentix Medical, Inc. | Orangeburg, NY, United States | Specification developer | 1 | November 15, 2018 | 0 | 0 | 0 | api.fda.gov |
| Covidien llc | Santa Clara, CA, United States | Specification developer | 1 | August 16, 2018 | 0 | 2 | 0 | api.fda.gov |
| Lucid Diagnostics, Inc. | Foxborough, MA, United States | Specification developer | 1 | February 24, 2023 | 0 | 1 | 0 | api.fda.gov |
| Teleflex LLC (NADC) | Olive Branch, MS, United States | Manufacturer, Repackager or relabeler | 1 | December 16, 1976 | 0 | 0 | 0 | api.fda.gov |
| Teleflex Medical LLC | Morrisville, NC, United States | Complaint file establishment, Specification developer | 1 | December 16, 1976 | 0 | 0 | 0 | api.fda.gov |
| Harwood Design, Inc. | Bristol, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Karl Storz Endovision, Inc. | Charlton, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Remedy Medical Manufacturing | Mesa, AZ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sage Product Development, Inc. | Foxborough, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.