Data / Medical devices / Tube, Double Lumen For Intestinal Decompression And/Or Intubation / United States
FDA-registered makers of Tube, Double Lumen For Intestinal Decompression And/Or Intubation in the United States: 5 establishments
5 establishments in the United States are registered with the FDA to make Tube, Double Lumen For Intestinal Decompression And/Or Intubation (product code FEG). 4 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Tube, Double Lumen For Intestinal Decompression And/Or Intubation
- Product code
- FEG
- Country
- United States
Makers of Tube, Double Lumen For Intestinal Decompression And/Or Intubation in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Cardinal Health | Hazelwood, MO, United States | Specification developer | 2 | May 17, 2004 | 0 | 0 | 0 | api.fda.gov |
| Axiom Medical, Inc. | Torrance, CA, United States | Manufacturer | 1 | July 19, 1977 | 0 | 0 | 0 | api.fda.gov |
| C.R. Bard, Inc. | Covington, GA, United States | Manufacturer | 1 | July 24, 1996 | 0 | 1 | 0 | api.fda.gov |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 1 | September 18, 2013 | 0 | 0 | 0 | api.fda.gov |
| Allwin Medical Devices, Inc. | Anaheim, CA, United States | Manufacturer for export | 0 | 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.