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Data / Medical devices / Stimulator, Spinal-Cord, Totally Implanted For Pain Relief / United States

FDA-registered makers of Stimulator, Spinal-Cord, Totally Implanted For Pain Relief in the United States: 30 establishments

30 establishments in the United States are registered with the FDA to make Stimulator, Spinal-Cord, Totally Implanted For Pain Relief (product code LGW). 10 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.

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Device
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
Product code
LGW
Country
United States

Makers of Stimulator, Spinal-Cord, Totally Implanted For Pain Relief in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Abbott MedicalPlano, TX, United StatesManufacturer01151api.fda.gov
Abbott MedicalArecibo, PR, United StatesManufacturer0100api.fda.gov
Boston Scientific CorporationSaint Paul, MN, United StatesManufacturer0100api.fda.gov
Boston Scientific CorporationDorado, PR, United StatesManufacturer0100api.fda.gov
Boston Scientific Neuromodulation CorporationValencia, CA, United StatesComplaint file establishment, Specification developer0151api.fda.gov
Medtronic NeuromodulationMinneapolis, MN, United StatesManufacturer01300api.fda.gov
Medtronic Puerto Rico Operations Co., JuncosJuncos, PR, United StatesManufacturer0100api.fda.gov
Medtronic Puerto Rico Operations Co., VillalbaVillalba, PR, United StatesManufacturer0100api.fda.gov
Medtronic Sofamor Danek Usa, Inc.Memphis, TN, United StatesManufacturer0100api.fda.gov
Nevro Corp.Redwood City, CA, United StatesManufacturer0100api.fda.gov
Benchmark Electronics, Inc.Winona, MN, United StatesContract manufacturer0000api.fda.gov
Cirtec MedicalBrooklyn Park, MN, United StatesContract manufacturer0000api.fda.gov
Eca Medical InstrumentsNewbury Park, CA, United StatesContract manufacturer0000api.fda.gov
Eptam Precision Molding Ma (a Division Of Eptam Precision)Lancaster, MA, United StatesContract manufacturer0000api.fda.gov
Fermatex Vascular Technologies D.B.A. Adam SpenceWall, NJ, United StatesContract manufacturer0000api.fda.gov
Fmi LLCLincolnshire, IL, United StatesContract manufacturer0000api.fda.gov
Heraeus Medical Components, LLCSaint Paul, MN, United StatesContract manufacturer0000api.fda.gov
JunoPacific, Inc.Brooklyn Park, MN, United StatesContract manufacturer0000api.fda.gov
Minnetronix, Inc.Saint Paul, MN, United StatesContract manufacturer0000api.fda.gov
Onanon, IncMilpitas, CA, United StatesContract manufacturer0000api.fda.gov
Oscor Inc.Palm Harbor, FL, United StatesContract manufacturer0000api.fda.gov
Pro-Tech Design & MFG., Inc.Santa Fe Springs, 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
Promed PharmaPlymouth, MN, United StatesContract manufacturer0000api.fda.gov
Quality Tech Services, LLCBloomington, MN, 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
Technical Services For Electronics, Inc.Jackson, MN, 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.