Data / Medical devices / Stimulator, Electrical, Implanted, For Essential Tremor / United States

FDA-registered makers of Stimulator, Electrical, Implanted, For Essential Tremor in the United States: 19 establishments

Name: FDA-registered makers of Stimulator, Electrical, Implanted, For Essential Tremor in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

19 establishments in the United States are registered with the FDA to make Stimulator, Electrical, Implanted, For Essential Tremor (product code PJS). 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, Electrical, Implanted, For Essential Tremor
Product code: PJS
Country: United States

Makers of Stimulator, Electrical, Implanted, For Essential Tremor in the United States

Maker	Location	Role	Source
Abbott Medical	Plano, TX, United States	Manufacturer	api.fda.gov
Abbott Medical	Arecibo, PR, United States	Manufacturer	api.fda.gov
Benchmark Electronics, Inc.	Winona, MN, United States	Contract manufacturer	api.fda.gov
Boston Scientific Corporation	Saint Paul, MN, United States	Manufacturer	api.fda.gov
Boston Scientific Corporation	Dorado, PR, United States	Manufacturer	api.fda.gov
Boston Scientific Neuromodulation Corporation	Valencia, CA, United States	Complaint file establishment, Specification developer	api.fda.gov
Eca Medical Instruments	Newbury Park, CA, United States	Contract manufacturer	api.fda.gov
Eptam Precision Molding Ma (a Division Of Eptam Precision)	Lancaster, MA, United States	Contract manufacturer	api.fda.gov
Medtronic Neuromodulation	Minneapolis, MN, United States	Manufacturer	api.fda.gov
Medtronic Puerto Rico Operations Co., Juncos	Juncos, PR, United States	Manufacturer	api.fda.gov
Medtronic Puerto Rico Operations Co., Villalba	Villalba, PR, United States	Manufacturer	api.fda.gov
Medtronic Sofamor Danek Usa, Inc.	Memphis, TN, United States	Manufacturer	api.fda.gov
Onanon, Inc	Milpitas, CA, United States	Contract manufacturer	api.fda.gov
PRO-TECH Design & Mfg, Inc.	Santa Fe Springs, CA, United States	Contract manufacturer	api.fda.gov
PRO-TECH Design & Mfg, Inc.	Arlington, TX, United States	Contract manufacturer	api.fda.gov
Promed Pharma	Plymouth, MN, United States	Contract manufacturer	api.fda.gov
Quality Tech Services, LLC	Bloomington, MN, United States	Contract manufacturer	api.fda.gov
Scapa Tapes North America, LLC	Knoxville, TN, United States	Contract manufacturer	api.fda.gov
Spartronics Watertown LLC	Watertown, SD, United States	Contract manufacturer	api.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.