Data / Medical devices / Stimulator, Peripheral Nerve, Implanted (Pain Relief)

Stimulator, Peripheral Nerve, Implanted (Pain Relief) (GZF): 20 FDA-registered makers in 3 countries

20 establishments in 3 countries are registered with the FDA to make Stimulator, Peripheral Nerve, Implanted (Pain Relief) (product code GZF, Class 2, 21 CFR 882.5870). 6 of them have a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 25 510(k) clearances under this code, the latest on August 26, 2026, and lists 2 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

GZF

Device class

2

Regulation

882.5870

Medical specialty

Neurology

Implant

Yes

Makers by country

Makers of Stimulator, Peripheral Nerve, Implanted (Pain Relief)

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

Updated August 26, 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.