Data / Medical devices / Stimulator, Nerve, Peripheral, Electric

Stimulator, Nerve, Peripheral, Electric (KOI): 41 FDA-registered makers in 16 countries

41 establishments in 16 countries are registered with the FDA to make Stimulator, Nerve, Peripheral, Electric (product code KOI, Class 2, 21 CFR 868.2775). 14 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 29 510(k) clearances under this code, the latest on May 22, 2026, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

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Product code

KOI

Device class

2

Regulation

868.2775

Medical specialty

Anesthesiology

Makers by country

Makers of Stimulator, Nerve, Peripheral, Electric

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 May 22, 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.