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Data / Medical devices / Stimulator, Spinal-Cord, Totally Implanted For Relief Of Pain Due To Diabetic Neuropathy / United States

FDA-registered makers of Stimulator, Spinal-Cord, Totally Implanted For Relief Of Pain Due To Diabetic Neuropathy in the United States: 18 establishments

18 establishments in the United States are registered with the FDA to make Stimulator, Spinal-Cord, Totally Implanted For Relief Of Pain Due To Diabetic Neuropathy (product code QRB). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Stimulator, Spinal-Cord, Totally Implanted For Relief Of Pain Due To Diabetic Neuropathy
Product code
QRB
Country
United States

Makers of Stimulator, Spinal-Cord, Totally Implanted For Relief Of Pain Due To Diabetic Neuropathy in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Abbott MedicalPlano, TX, United StatesManufacturer0000api.fda.gov
Abbott MedicalArecibo, PR, United StatesManufacturer0000api.fda.gov
Benchmark Electronics, Inc.Winona, MN, United StatesContract manufacturer0000api.fda.gov
Boston Scientific CorporationSaint Paul, MN, United StatesManufacturer0000api.fda.gov
Boston Scientific CorporationDorado, PR, United StatesManufacturer0000api.fda.gov
Boston Scientific Neuromodulation CorporationValencia, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Eptam Precision Molding Ma (a Division Of Eptam Precision)Lancaster, MA, United StatesContract manufacturer0000api.fda.gov
Medtronic NeuromodulationMinneapolis, MN, United StatesManufacturer0000api.fda.gov
Medtronic Puerto Rico Operations Co., JuncosJuncos, PR, United StatesManufacturer0000api.fda.gov
Medtronic Puerto Rico Operations Co., VillalbaVillalba, PR, United StatesManufacturer0000api.fda.gov
Medtronic Sofamor Danek Usa, Inc.Memphis, TN, United StatesManufacturer0000api.fda.gov
Nevro Corp.Redwood City, CA, United StatesManufacturer0000api.fda.gov
Onanon, IncMilpitas, CA, United StatesContract manufacturer0000api.fda.gov
Pro-Tech Design & MFG., Inc.Santa Fe Springs, CA, United StatesContract manufacturer0000api.fda.gov
PRO-TECH Design & Mfg, Inc.Arlington, TX, United StatesContract manufacturer0000api.fda.gov
Scapa Tapes North America, LLCKnoxville, TN, United StatesContract manufacturer0000api.fda.gov
Spartronics Watertown LLCWatertown, SD, United StatesContract manufacturer0000api.fda.gov
VestaFranklin, WI, 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.