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Data / Medical devices / Implanted Subcortical Electrical Stimulator (Motor Disorders) / United States

FDA-registered makers of Implanted Subcortical Electrical Stimulator (Motor Disorders) in the United States: 5 establishments

5 establishments in the United States are registered with the FDA to make Implanted Subcortical Electrical Stimulator (Motor Disorders) (product code MRU). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.

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Device
Implanted Subcortical Electrical Stimulator (Motor Disorders)
Product code
MRU
Country
United States

Makers of Implanted Subcortical Electrical Stimulator (Motor Disorders) in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Medtronic NeuromodulationMinneapolis, MN, United StatesManufacturer0021api.fda.gov
Medtronic Puerto Rico Operations Co., JuncosJuncos, PR, United StatesManufacturer0000api.fda.gov
Medtronic Puerto Rico Operations Co., VillalbaVillalba, PR, United StatesManufacturer0000api.fda.gov
Quality Tech Services, LLCBloomington, MN, United StatesContract manufacturer0000api.fda.gov
Technical Services For Electronics, Inc.Jackson, MN, United StatesContract manufacturer0000api.fda.gov

Updated November 3, 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.