Data / Medical devices / Temporary Carotid Catheter For Embolic Capture / United States
FDA-registered makers of Temporary Carotid Catheter For Embolic Capture in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Temporary Carotid Catheter For Embolic Capture (product code NTE). 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
- Temporary Carotid Catheter For Embolic Capture
- Product code
- NTE
- Country
- United States
Makers of Temporary Carotid Catheter For Embolic Capture in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| ev3, Inc. | Plymouth, MN, United States | Manufacturer, Specification developer | 3 | October 27, 2011 | 0 | 0 | 0 | api.fda.gov |
| Cardiovascular Systems Incorporated | Saint Paul, MN, United States | Complaint file establishment, Manufacturer | 2 | March 3, 2021 | 0 | 1 | 1 | api.fda.gov |
| Abbott Vascular | Temecula, CA, United States | Complaint file establishment, Manufacturer | 1 | July 25, 2019 | 0 | 1 | 0 | api.fda.gov |
| Abbott Vascular | Santa Clara, CA, United States | Specification developer | 1 | July 25, 2019 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Maple Grove, MN, United States | Manufacturer, Specification developer | 1 | April 11, 2023 | 0 | 2 | 1 | api.fda.gov |
| Boston Scientific Corporation | Coventry, RI, United States | Manufacturer | 1 | April 11, 2023 | 0 | 0 | 0 | api.fda.gov |
| Cordis US Corp. | Miami Lakes, FL, United States | Complaint file establishment, Specification developer | 1 | April 6, 2022 | 0 | 1 | 1 | api.fda.gov |
| MicroVention, Inc. | Aliso Viejo, CA, United States | Manufacturer | 1 | April 27, 2023 | 0 | 0 | 0 | api.fda.gov |
| Contego Medical, Inc | Raleigh, NC, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lake Region Medical | Chaska, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sterigenics U.S., LLC | Queensbury, NY, United States | Contract sterilizer, Manufacturer for export | 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.