Data / Medical devices / Stopcock, I.V. Set / United States
FDA-registered makers of Stopcock, I.V. Set in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Stopcock, I.V. Set (product code FMG). 10 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.
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- Device
- Stopcock, I.V. Set
- Product code
- FMG
- Country
- United States
Makers of Stopcock, I.V. Set in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Icu Medical, Inc | Salt Lake City, UT, United States | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | 3 | February 13, 2008 | 0 | 0 | 0 | api.fda.gov |
| Icu Medical, Inc. | San Clemente, CA, United States | Complaint file establishment, Specification developer | 3 | February 25, 2009 | 0 | 16 | 2 | api.fda.gov |
| ICU Medical, Inc. | Dublin, OH, United States | Manufacturer | 3 | April 22, 1996 | 0 | 0 | 0 | api.fda.gov |
| Baxter Healthcare Corporation | Round Lake, IL, United States | Complaint file establishment, Specification developer | 2 | March 10, 2023 | 0 | 5 | 0 | api.fda.gov |
| Avid Medical, Inc. A Medical Action Ind. Company 305 | Toano, VA, United States | Manufacturer, Repackager or relabeler | 1 | October 7, 1995 | 0 | 0 | 0 | api.fda.gov |
| Carefusion | San Diego, CA, United States | Specification developer | 1 | January 13, 1998 | 0 | 0 | 0 | api.fda.gov |
| Procedure Products, Inc. | Vancouver, WA, United States | Manufacturer | 1 | September 5, 1984 | 0 | 0 | 0 | api.fda.gov |
| Quest Medical, Inc. | Allen, TX, United States | Manufacturer | 1 | May 10, 2006 | 0 | 0 | 0 | api.fda.gov |
| Vygon Usa | Lansdale, PA, United States | Specification developer | 1 | September 11, 2001 | 0 | 0 | 0 | api.fda.gov |
| Vygon MFG | Dover, NH, United States | Manufacturer | 1 | September 11, 2001 | 0 | 1 | 0 | api.fda.gov |
| Becton Dickinson | Franklin Lakes, NJ, United States | Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Becton, Dickinson And Company | Irvine, CA, United States | Specification developer | 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.