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Data / Medical devices / Endoscope, Neurological / United States

FDA-registered makers of Endoscope, Neurological in the United States: 23 establishments

23 establishments in the United States are registered with the FDA to make Endoscope, Neurological (product code GWG). 12 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Endoscope, Neurological
Product code
GWG
Country
United States

Makers of Endoscope, Neurological in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Karl Storz Endoscopy-America, Inc.Auburn, MA, United StatesContract manufacturer, Repackager or relabeler12April 17, 2018000api.fda.gov
Medtronic NeurosurgeryFort Worth, TX, United StatesSpecification developer7April 20, 2001030api.fda.gov
Clarus Medical, LLC.Minneapolis, MN, United StatesManufacturer4November 21, 2023000api.fda.gov
Penumbra, Inc.Alameda, CA, United StatesManufacturer3August 14, 2017000api.fda.gov
Penumbra Inc.Roseville, CA, United StatesManufacturer3August 14, 2017000api.fda.gov
Penumbra Inc.Salt Lake City, UT, United StatesManufacturer3August 14, 2017000api.fda.gov
Penumbra Inc.Livermore, CA, United StatesManufacturer3August 14, 2017000api.fda.gov
Rebound Therapeutics, CorporationIrvine, CA, United StatesManufacturer3April 9, 2025000api.fda.gov
Stryker EndoscopySan Jose, CA, United StatesComplaint file establishment, Manufacturer, Specification developer2June 4, 2026000api.fda.gov
ClearPoint Neuro Inc.Carlsbad, CA, United StatesManufacturer1November 20, 2018000api.fda.gov
Highridge Medical, LLCWestminster, CO, United StatesSpecification developer1January 27, 1999000api.fda.gov
Stryker InstrumentsPortage, MI, United StatesComplaint file establishment, Specification developer1May 8, 2026000api.fda.gov
Karl Storz Endovision, Inc.Charlton, MA, United StatesContract manufacturer0000api.fda.gov
Karl Storz Imaging, Inc.Goleta, CA, United StatesContract manufacturer0000api.fda.gov
Kimball Solutions Jasper, Inc.Jasper, IN, United StatesContract manufacturer0000api.fda.gov
Linemaster Switch Corp.Woodstock, CT, United StatesContract manufacturer0000api.fda.gov
Olive Branch Distribution CenterOlive Branch, MS, United StatesContract manufacturer0000api.fda.gov
Primo Medical Group, IncW Bridgewater, MA, United StatesContract manufacturer0000api.fda.gov
Richard Wolf Medical Instruments Corp.Vernon Hills, IL, United StatesContract manufacturer0000api.fda.gov
Scientific Molding Corporation, Ltd. Dba SMC Ltd.Santa Rosa, CA, United StatesContract manufacturer0000api.fda.gov
Stryker Puerto Rico, LLC.Arroyo, PR, United StatesContract manufacturer0000api.fda.gov
Siemens Healthcare Diagnostics Inc.Tarrytown, NY, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Siemens Healthcare Diagnostics Inc.E Walpole, MA, United StatesManufacturer0000api.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.