Data / Medical devices / Catheter, Umbilical Artery / United States
FDA-registered makers of Catheter, Umbilical Artery in the United States: 5 establishments
5 establishments in the United States are registered with the FDA to make Catheter, Umbilical Artery (product code FOS). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Catheter, Umbilical Artery
- Product code
- FOS
- Country
- United States
Makers of Catheter, Umbilical Artery 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 | 6 | April 17, 2013 | 0 | 0 | 0 | api.fda.gov |
| Footprint Medical Inc. | San Antonio, TX, United States | Manufacturer | 3 | March 1, 2012 | 0 | 0 | 0 | api.fda.gov |
| Utah Medical Products, Inc. | Midvale, UT, United States | Manufacturer | 3 | August 2, 1994 | 0 | 0 | 0 | api.fda.gov |
| Gamamed Vascular Systems Inc. | Loveland, CO, United States | Manufacturer, Repackager or relabeler | 1 | May 6, 2021 | 0 | 0 | 0 | api.fda.gov |
| Haolang Medical Usa Corporation | Clyde Hill, WA, United States | Specification developer | 1 | May 6, 2021 | 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.