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Data / Medical devices / Catheter, Percutaneous, Neurovasculature / United States

FDA-registered makers of Catheter, Percutaneous, Neurovasculature in the United States: 30 establishments

30 establishments in the United States are registered with the FDA to make Catheter, Percutaneous, Neurovasculature (product code QJP). 25 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
Catheter, Percutaneous, Neurovasculature
Product code
QJP
Country
United States

Makers of Catheter, Percutaneous, Neurovasculature in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Stryker NeurovascularFremont, CA, United StatesComplaint file establishment, Specification developer10October 9, 2026020api.fda.gov
Balt Usa, LLCIrvine, CA, United StatesComplaint file establishment, Manufacturer6July 13, 2026000api.fda.gov
Imperative Care Inc.Campbell, CA, United StatesComplaint file establishment, Manufacturer, Specification developer6August 28, 2026000api.fda.gov
Cerenovus, Inc.Miami, FL, United StatesSpecification developer5October 16, 2024000api.fda.gov
Penumbra, Inc.Alameda, CA, United StatesManufacturer5December 11, 2024000api.fda.gov
Penumbra Inc.Roseville, CA, United StatesManufacturer5December 11, 2024000api.fda.gov
Penumbra Inc.Salt Lake City, UT, United StatesManufacturer5December 11, 2024000api.fda.gov
Penumbra Inc.Livermore, CA, United StatesManufacturer5December 11, 2024000api.fda.gov
Route 92 Medical, Head QuartersSan Mateo, CA, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler5September 16, 2026011api.fda.gov
Route 92 Medical, West JordanW Jordan, UT, United StatesManufacturer, Repackager or relabeler5September 16, 2026000api.fda.gov
Micro Therapeutics, Inc. Dba Ev3 NeurovascularIrvine, CA, United StatesComplaint file establishment, Manufacturer4January 14, 2025000api.fda.gov
Maduro Medical, Inc.Los Gatos, CA, United StatesComplaint file establishment, Manufacturer3April 9, 2026000api.fda.gov
Micro Therapeutics, Inc. Dba Ev3 NeurovascularIrvine, CA, United StatesSpecification developer3January 2, 2025000api.fda.gov
Piraeus Medical, Inc.Maple Grove, MN, United StatesManufacturer3September 4, 2026000api.fda.gov
Stryker NeurovascularSalt Lake City, UT, United StatesManufacturer3December 19, 2024010api.fda.gov
MicroVention, Inc.Aliso Viejo, CA, United StatesManufacturer, Repackager or relabeler, Specification developer2May 16, 2024000api.fda.gov
Q'apel Medical, Inc.Fremont, CA, United StatesManufacturer2November 20, 2024000api.fda.gov
Scientia VascularWest Valley City, UT, United StatesManufacturer2December 4, 2024010api.fda.gov
Wallaby MedicalLaguna Hills, CA, United StatesSpecification developer2August 18, 2026000api.fda.gov
Alembic LLCMountain View, CA, United StatesComplaint file establishment, Manufacturer1January 14, 2025000api.fda.gov
Crossroads NeurovascularLake Forest, CA, United StatesSpecification developer1May 9, 2025000api.fda.gov
Kaneka Americas Holding IncNewark, CA, United StatesComplaint file establishment, Specification developer1January 5, 2026000api.fda.gov
Sonorous NV, Inc.Lake Forest, CA, United StatesSpecification developer1April 21, 2026000api.fda.gov
Toro Neurovascular, Inc.Irvine, CA, United StatesSpecification developer1January 16, 2026000api.fda.gov
VesalioSan Diego, CA, United StatesComplaint file establishment, Specification developer1January 6, 2026000api.fda.gov
BiosealPlacentia, CA, United StatesContract manufacturer0000api.fda.gov
CPE1, LLC DBA Greatbatch MedicalSouthwest Ranches, FL, United StatesContract manufacturer0000api.fda.gov
Eosolutions, Corp.Miramar, FL, United StatesSpecification developer0000api.fda.gov
Lake Region MedicalTrenton, GA, United StatesContract manufacturer0000api.fda.gov
M4D LLCLake Forest, CA, United StatesContract manufacturer0000api.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.