Data / Medical devices / Tubes, Vacuum Sample, With Anticoagulant / United States
FDA-registered makers of Tubes, Vacuum Sample, With Anticoagulant in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Tubes, Vacuum Sample, With Anticoagulant (product code GIM). 10 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
- Tubes, Vacuum Sample, With Anticoagulant
- Product code
- GIM
- Country
- United States
Makers of Tubes, Vacuum Sample, With Anticoagulant 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 | 8 | July 10, 1992 | 0 | 0 | 0 | api.fda.gov |
| Cardinal Health | Norfolk, NE, United States | Manufacturer | 6 | January 8, 1992 | 0 | 0 | 0 | api.fda.gov |
| Becton Dickinson | Franklin Lakes, NJ, United States | Specification developer | 2 | November 27, 2023 | 0 | 0 | 0 | api.fda.gov |
| BD Puerto Rico LLC | Juncos, PR, United States | Manufacturer | 1 | November 27, 2023 | 0 | 0 | 0 | api.fda.gov |
| Becton, Dickinson & Co. | Broken Bow, NE, United States | Manufacturer | 1 | August 25, 2023 | 0 | 0 | 0 | api.fda.gov |
| Edwards Lifesciences Technology Sarl | Anasco, PR, United States | Manufacturer | 1 | November 27, 2023 | 0 | 0 | 0 | api.fda.gov |
| Greiner Bio-One North America, Inc. | Monroe, NC, United States | Manufacturer | 1 | May 2, 1997 | 0 | 7 | 0 | api.fda.gov |
| Porex Corporation | Fairburn, GA, United States | Manufacturer | 1 | November 2, 1977 | 0 | 0 | 0 | api.fda.gov |
| Streck LLC | La Vista, NE, United States | Manufacturer | 1 | July 31, 2008 | 0 | 1 | 0 | api.fda.gov |
| Streck LLC | La Vista, NE, United States | Manufacturer | 1 | July 31, 2008 | 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.