Data / Medical devices / Tube, Collection, Capillary Blood / United States
FDA-registered makers of Tube, Collection, Capillary Blood in the United States: 15 establishments
15 establishments in the United States are registered with the FDA to make Tube, Collection, Capillary Blood (product code GIO). 1 has 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, Collection, Capillary Blood
- Product code
- GIO
- Country
- United States
Makers of Tube, Collection, Capillary Blood in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Becton, Dickinson & Co. | Sparks, MD, United States | Repackager or relabeler, Specification developer | 1 | December 1, 1988 | 0 | 0 | 0 | api.fda.gov |
| Becton Dickinson | Franklin Lakes, NJ, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bionostics, Inc. | Devens, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Drummond Scientific Co. | Broomall, PA, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| DWK Life Sciences, LLC. | Rockwood, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Drucker Diagnostics, LLC | Philipsburg, PA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Newtrans International Company | Nashville, TN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Opti Medical Systems Inc. | Roswell, GA, United States | Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Polymer Technology Systems | Whitestown, IN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ramko Injection Inc | Hemet, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Healthcare Diagnostics Inc | East Walpole, MA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Healthcare Diagnostics Inc. | Tarrytown, NY, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Trademark Plastics Inc. | Riverside, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vetirus, LLC | Naples, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Volusol | Tooele, UT, United States | Manufacturer | 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.