Data / Medical devices / Tubing, Fluid Delivery / United States
FDA-registered makers of Tubing, Fluid Delivery in the United States: 16 establishments
16 establishments in the United States are registered with the FDA to make Tubing, Fluid Delivery (product code FPK). 11 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.
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- Device
- Tubing, Fluid Delivery
- Product code
- FPK
- Country
- United States
Makers of Tubing, Fluid Delivery in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bayer Medical Care Inc. | Indianola, PA, United States | Complaint file establishment, Manufacturer, Manufacturer for export, Specification developer | 3 | August 2, 2013 | 0 | 0 | 0 | api.fda.gov |
| Argon Medical Devices Inc. | Athens, TX, United States | Manufacturer, Repackager or relabeler | 1 | May 16, 1978 | 0 | 0 | 0 | api.fda.gov |
| Centurion Medical Products, LP | Williamston, MI, United States | Specification developer | 1 | April 1, 1991 | 0 | 0 | 0 | api.fda.gov |
| Coeur, Inc.(a Wholly Owned Subsidiary Of Illinois Tool Works Inc.) | Washington, NC, United States | Manufacturer | 1 | February 9, 2007 | 0 | 0 | 0 | api.fda.gov |
| Douglas Medical Products, Inc | Mundelein, IL, United States | Complaint file establishment, Specification developer | 1 | May 14, 1992 | 0 | 0 | 0 | api.fda.gov |
| Emed Technologies Corporation | El Dorado Hills, CA, United States | Specification developer | 1 | January 28, 1994 | 0 | 0 | 0 | api.fda.gov |
| Icu Medical, Inc. | Lake Forest, IL, United States | Complaint file establishment, Specification developer | 1 | October 3, 1994 | 0 | 1 | 0 | api.fda.gov |
| Merit Medical Systems, Inc. | South Jordan, UT, United States | Specification developer | 1 | January 30, 1989 | 0 | 1 | 0 | api.fda.gov |
| Quest Medical, Inc. | Allen, TX, United States | Manufacturer | 1 | May 14, 1980 | 0 | 0 | 0 | api.fda.gov |
| Summit Medical, Inc. | Franklin, MA, United States | Specification developer | 1 | February 5, 1993 | 0 | 0 | 0 | api.fda.gov |
| Vygon MFG | Dover, NH, United States | Manufacturer | 1 | November 7, 1988 | 0 | 0 | 0 | api.fda.gov |
| Busse Hospital Disposables | Hauppauge, NY, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cardinal Health | Hazelwood, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Isomedix Operations Inc. | Chester, NY, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medtronic Minimed | Northridge, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Vygon Usa | Lansdale, PA, 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.