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Data / Medical devices / Catheter, Thrombus Retriever / United States

FDA-registered makers of Catheter, Thrombus Retriever in the United States: 28 establishments

28 establishments in the United States are registered with the FDA to make Catheter, Thrombus Retriever (product code NRY). 20 have a 510(k) clearance or PMA approval on file and 8 have a recall event. FDA data exported November 2, 2026.

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Device
Catheter, Thrombus Retriever
Product code
NRY
Country
United States

Makers of Catheter, Thrombus Retriever in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Penumbra, Inc.Alameda, CA, United StatesManufacturer, Manufacturer for export25June 10, 2026042api.fda.gov
Penumbra Inc.Roseville, CA, United StatesManufacturer, Manufacturer for export25June 10, 2026000api.fda.gov
Penumbra Inc.Salt Lake City, UT, United StatesManufacturer, Manufacturer for export25June 10, 2026000api.fda.gov
Penumbra Inc.Livermore, CA, United StatesManufacturer, Manufacturer for export25June 10, 2026010api.fda.gov
Micro Therapeutics, Inc. Dba Ev3 NeurovascularIrvine, CA, United StatesComplaint file establishment, Manufacturer, Manufacturer for export16April 30, 2025000api.fda.gov
Micro Therapeutics, Inc. Dba Ev3 NeurovascularIrvine, CA, United StatesSpecification developer10October 29, 2024000api.fda.gov
Stryker NeurovascularFremont, CA, United StatesComplaint file establishment, Manufacturer, Specification developer10August 2, 2019050api.fda.gov
Imperative Care Inc.Campbell, CA, United StatesComplaint file establishment, Manufacturer, Specification developer7October 30, 2025011api.fda.gov
Alembic LLCMountain View, CA, United StatesComplaint file establishment, Manufacturer6April 30, 2025000api.fda.gov
Cerenovus, Inc.Miami, FL, United StatesSpecification developer6August 13, 2026000api.fda.gov
Route 92 Medical, Head QuartersSan Mateo, CA, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler3May 19, 2025011api.fda.gov
Route 92 Medical, West JordanW Jordan, UT, United StatesManufacturer, Repackager or relabeler3May 19, 2025000api.fda.gov
Stryker NeurovascularSalt Lake City, UT, United StatesManufacturer3June 12, 2015000api.fda.gov
Balt Usa, LLCIrvine, CA, United StatesComplaint file establishment, Manufacturer2June 3, 2025000api.fda.gov
MicroVention, Inc.Aliso Viejo, CA, United StatesManufacturer, Repackager or relabeler, Specification developer2March 31, 2022010api.fda.gov
Wallaby MedicalLaguna Hills, CA, United StatesSpecification developer2October 1, 2024000api.fda.gov
Maduro Medical, Inc.Los Gatos, CA, United StatesComplaint file establishment, Manufacturer1September 14, 2026000api.fda.gov
Q'apel Medical, Inc.Fremont, CA, United StatesManufacturer1May 7, 2026011api.fda.gov
Scientia VascularWest Valley City, UT, United StatesManufacturer1September 20, 2023010api.fda.gov
VesalioSan Diego, CA, United StatesComplaint file establishment, Manufacturer for export, Specification developer1November 10, 2025000api.fda.gov
CPE1, LLC DBA Greatbatch MedicalSouthwest Ranches, FL, United StatesContract manufacturer0000api.fda.gov
Gravity Medical TechnologyLake Forest, CA, United StatesManufacturer for export0000api.fda.gov
Infinity Neuro, LLCLake Forest, CA, United StatesManufacturer for export0000api.fda.gov
Merit Medical Systems, Inc.South Jordan, UT, United StatesContract manufacturer0000api.fda.gov
NeuroVasc Technologies, Inc.Irvine, CA, United StatesManufacturer for export0000api.fda.gov
Rapidpulse, Inc.Miami, FL, United StatesManufacturer for export0000api.fda.gov
Scientific Molding Corporation, Ltd. Dba SMC Ltd.Santa Rosa, CA, United StatesContract manufacturer0000api.fda.gov
Spartronics Strongsville, Inc.Strongsville, OH, 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.