Data / Medical devices / Guide, Wire, Catheter, Neurovasculature / United States
FDA-registered makers of Guide, Wire, Catheter, Neurovasculature in the United States: 13 establishments
13 establishments in the United States are registered with the FDA to make Guide, Wire, Catheter, Neurovasculature (product code MOF). 10 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Guide, Wire, Catheter, Neurovasculature
- Product code
- MOF
- Country
- United States
Makers of Guide, Wire, Catheter, Neurovasculature in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Scientia Vascular | West Valley City, UT, United States | Manufacturer | 6 | August 6, 2026 | 0 | 0 | 0 | api.fda.gov |
| Arbor Endovascular | San Jose, CA, United States | Complaint file establishment, Specification developer | 5 | August 14, 2026 | 0 | 0 | 0 | api.fda.gov |
| MicroVention, Inc. | Aliso Viejo, CA, United States | Manufacturer, Repackager or relabeler, Specification developer | 4 | July 2, 2020 | 0 | 1 | 0 | api.fda.gov |
| Stryker Neurovascular | Fremont, CA, United States | Specification developer | 2 | September 25, 2020 | 0 | 1 | 0 | api.fda.gov |
| Stryker Neurovascular | Salt Lake City, UT, United States | Manufacturer | 2 | September 25, 2020 | 0 | 0 | 0 | api.fda.gov |
| Balt Usa, LLC | Irvine, CA, United States | Manufacturer | 1 | October 4, 2018 | 0 | 0 | 0 | api.fda.gov |
| Cerenovus, Inc. | Miami, FL, United States | Specification developer | 1 | February 24, 2014 | 0 | 0 | 0 | api.fda.gov |
| Cerenovus, Inc. | Raynham, MA, United States | Manufacturer | 1 | February 24, 2014 | 0 | 0 | 0 | api.fda.gov |
| Imperative Care Inc. | Campbell, CA, United States | Complaint file establishment, Specification developer | 1 | August 26, 2025 | 0 | 0 | 0 | api.fda.gov |
| Piraeus Medical, Inc. | Maple Grove, MN, United States | Manufacturer | 1 | August 27, 2026 | 0 | 0 | 0 | api.fda.gov |
| Micro Therapeutics, Inc. Dba Ev3 Neurovascular | Irvine, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Micro Therapeutics, Inc. Dba Ev3 Neurovascular | Irvine, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| NeedleTech Products, Inc. | N Attleboro, MA, 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.