Data / Medical devices / Stent, Carotid / United States
FDA-registered makers of Stent, Carotid in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Stent, Carotid (product code NIM). 7 have a 510(k) clearance or PMA approval on file and 5 have a recall event. FDA data exported November 2, 2026.
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- Device
- Stent, Carotid
- Product code
- NIM
- Country
- United States
Makers of Stent, Carotid in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Abbott Vascular | Temecula, CA, United States | Complaint file establishment, Manufacturer | 0 | 2 | 3 | 0 | api.fda.gov | |
| Abbott Vascular | Santa Clara, CA, United States | Specification developer | 0 | 2 | 0 | 0 | api.fda.gov | |
| Boston Scientific Corporation | Maple Grove, MN, United States | Specification developer | 0 | 1 | 2 | 1 | api.fda.gov | |
| Contego Medical, Inc | Raleigh, NC, United States | Complaint file establishment, Specification developer | 0 | 1 | 2 | 0 | api.fda.gov | |
| Cordis US Corp. | Miami Lakes, FL, United States | Complaint file establishment, Specification developer | 0 | 1 | 2 | 1 | api.fda.gov | |
| MicroVention, Inc. | Aliso Viejo, CA, United States | Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| ev3, Inc. | Plymouth, MN, United States | Manufacturer | 0 | 1 | 1 | 0 | api.fda.gov | |
| Maruho Relucent, Inc | Santa Rosa, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Murray, Inc. | Lake Zurich, IL, 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.