Data / Medical devices / Device, Hemostasis, Vascular / United States
FDA-registered makers of Device, Hemostasis, Vascular in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Device, Hemostasis, Vascular (product code MGB). 8 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
- Device, Hemostasis, Vascular
- Product code
- MGB
- Country
- United States
Makers of Device, Hemostasis, Vascular in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Abbott Vascular | Santa Clara, CA, United States | Specification developer | 0 | 2 | 0 | 0 | api.fda.gov | |
| Cordis US Corp. | Miami Lakes, FL, United States | Complaint file establishment, Specification developer | 0 | 2 | 2 | 0 | api.fda.gov | |
| Teleflex Medical LLC | Morrisville, NC, United States | Complaint file establishment, Specification developer | 0 | 2 | 1 | 0 | api.fda.gov | |
| Vascular Solutions LLC | Maple Grove, MN, United States | Manufacturer | 0 | 2 | 0 | 0 | api.fda.gov | |
| Cardiva Medical, Inc. | Santa Clara, CA, United States | Complaint file establishment, Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Cordis US Corp. | Santa Clara, CA, United States | Manufacturer, Specification developer | 0 | 1 | 1 | 0 | api.fda.gov | |
| St. Jude Medical, Cardiology Division, Inc. | Plymouth, MN, United States | Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Terumo Medical Corp. | Somerset, NJ, United States | Manufacturer for export, Specification developer | 0 | 1 | 1 | 0 | api.fda.gov | |
| Isomedix Operations Inc. | S Plainfield, NJ, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rose Medical | Grand Rapids, MI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tesco Associates, Inc. | Tyngsboro, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Terumo Puerto Rico LLC | Caguas, PR, 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.