Data / Medical devices / Tube, Feeding / United States
FDA-registered makers of Tube, Feeding in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Tube, Feeding (product code FPD). 9 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 3, 2026.
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- Device
- Tube, Feeding
- Product code
- FPD
- Country
- United States
Makers of Tube, Feeding in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Avanos Medical, Inc. | Alpharetta, GA, United States | Complaint file establishment, Specification developer | 4 | April 22, 2010 | 0 | 1 | 0 | api.fda.gov |
| Kentec Medical, LLC | Irvine, CA, United States | Complaint file establishment, Specification developer | 3 | January 18, 2019 | 0 | 2 | 0 | api.fda.gov |
| Covidien | Lafayette, CO, United States | Specification developer | 1 | July 16, 1976 | 0 | 0 | 0 | api.fda.gov |
| Duopross Meditech Corporation | Farmingdale, NY, United States | Specification developer | 1 | June 14, 2010 | 0 | 0 | 0 | api.fda.gov |
| Multi-Med, Inc. | Keene, NH, United States | Contract manufacturer, Manufacturer | 1 | May 23, 1989 | 0 | 0 | 0 | api.fda.gov |
| Teleflex LLC (NADC) | Olive Branch, MS, United States | Manufacturer, Repackager or relabeler | 1 | May 23, 1997 | 0 | 0 | 0 | api.fda.gov |
| Teleflex Medical LLC | Morrisville, NC, United States | Complaint file establishment, Specification developer | 1 | May 23, 1997 | 0 | 0 | 0 | api.fda.gov |
| Vygon Usa | Lansdale, PA, United States | Specification developer | 1 | September 15, 2006 | 0 | 0 | 0 | api.fda.gov |
| Vygon MFG | Dover, NH, United States | Manufacturer | 1 | September 15, 2006 | 0 | 0 | 0 | api.fda.gov |
| Actuated Medical, Inc. | Bellefonte, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gravitas Medical, Inc. | Berkeley, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Generica Medical International | La Verne, CA, United States | Complaint file establishment, 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.