Data / Medical devices / Gastrointestinal Tubes With Enteral Specific Connectors / United States
FDA-registered makers of Gastrointestinal Tubes With Enteral Specific Connectors in the United States: 16 establishments
16 establishments in the United States are registered with the FDA to make Gastrointestinal Tubes With Enteral Specific Connectors (product code PIF). 15 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 3, 2026.
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- Device
- Gastrointestinal Tubes With Enteral Specific Connectors
- Product code
- PIF
- Country
- United States
Makers of Gastrointestinal Tubes With Enteral Specific Connectors 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 | 5 | May 19, 2022 | 0 | 0 | 0 | api.fda.gov |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 3 | December 4, 2019 | 0 | 0 | 0 | api.fda.gov |
| Vesco Medical LLC | New Albany, OH, United States | Specification developer | 3 | November 2, 2023 | 0 | 0 | 0 | api.fda.gov |
| Xeridiem Medical Devices | Tucson, AZ, United States | Contract manufacturer, Manufacturer | 3 | October 6, 2023 | 0 | 1 | 0 | api.fda.gov |
| Boston Scientific Corporation | Marlborough, MA, United States | Complaint file establishment, Specification developer | 2 | June 17, 2016 | 0 | 3 | 0 | api.fda.gov |
| Syncro Medical Innovations, Inc. | Macon, GA, United States | Specification developer | 2 | November 5, 2020 | 0 | 0 | 0 | api.fda.gov |
| U Deliver Medical L.L.C. | Hopkins, MN, United States | Complaint file establishment, Specification developer | 2 | May 31, 2019 | 0 | 0 | 0 | api.fda.gov |
| Vonco Products, LLC | Trevor, WI, United States | Manufacturer | 2 | July 10, 2023 | 0 | 0 | 0 | api.fda.gov |
| Applied Medical Technology, Inc. | Brecksville, OH, United States | Manufacturer | 1 | January 29, 2015 | 0 | 1 | 0 | api.fda.gov |
| Avanos Medical, Inc. | Alpharetta, GA, United States | Specification developer | 1 | November 20, 2014 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Spencer, IN, United States | Manufacturer, Manufacturer for export | 1 | May 29, 2015 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corp., Marina Bay Cust. Fulfillment Center | Quincy, MA, United States | Manufacturer | 1 | May 29, 2015 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Coventry, RI, United States | Manufacturer | 1 | May 29, 2015 | 0 | 0 | 0 | api.fda.gov |
| KB Medical (group) Inc. | Irvine, CA, United States | Specification developer | 1 | November 16, 2021 | 0 | 0 | 0 | api.fda.gov |
| Zevex, Inc. | Salt Lake City, UT, United States | Specification developer | 1 | January 8, 2015 | 0 | 1 | 0 | api.fda.gov |
| ENvue Medical (USA) Inc. | Arlington Heights, IL, United States | Specification developer | 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.