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Data / Medical devices / Dorsal Root Ganglion Stimulator For Pain Relief / United States

FDA-registered makers of Dorsal Root Ganglion Stimulator For Pain Relief in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make Dorsal Root Ganglion Stimulator For Pain Relief (product code PMP). 1 has 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
Dorsal Root Ganglion Stimulator For Pain Relief
Product code
PMP
Country
United States

Makers of Dorsal Root Ganglion Stimulator For Pain Relief in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Abbott MedicalPlano, TX, United StatesManufacturer0120api.fda.gov
Accumold LLCAnkeny, IA, United StatesContract manufacturer0000api.fda.gov
Benchmark Electronics, Inc.Winona, MN, United StatesContract manufacturer0000api.fda.gov
Eptam Precision Molding Ma (a Division Of Eptam Precision)Lancaster, MA, United StatesContract manufacturer0000api.fda.gov
Extrumed, Inc.Corona, 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

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.