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Data / Medical devices / Stimulator, Nerve, Ac-Powered

Stimulator, Nerve, Ac-Powered (BXM): 3 FDA-registered makers in 1 country

3 establishments in 1 country are registered with the FDA to make Stimulator, Nerve, Ac-Powered (product code BXM, Class 2, 21 CFR 868.2775). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 4 510(k) clearances under this code, the latest on October 16, 2001, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
BXM
Device class
2
Regulation
868.2775
Medical specialty
Anesthesiology

Makers by country

CountryMakers
United States3

Makers of Stimulator, Nerve, Ac-Powered

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.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Globus Medical, Inc.Memphis, TN, United StatesManufacturer1October 16, 2001000api.fda.gov
Nuvasive, Inc.San Diego, CA, United StatesManufacturer1October 16, 2001000api.fda.gov
Amrex-Zetron, Inc.Paramount, CA, United StatesManufacturer0000api.fda.gov

Updated October 16, 2001. 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.