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Data / Medical devices / Stimulator, Muscle, Powered, Dental

Stimulator, Muscle, Powered, Dental (NUW): 4 FDA-registered makers in 3 countries

4 establishments in 3 countries are registered with the FDA to make Stimulator, Muscle, Powered, Dental (product code NUW, Class 2, 21 CFR 890.5850). 4 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 9 510(k) clearances under this code, the latest on May 9, 2025, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
NUW
Device class
2
Regulation
890.5850
Medical specialty
Physical Medicine

Makers by country

CountryMakers
Japan2
United States1
Bulgaria1

Makers of Stimulator, Muscle, Powered, Dental

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
Myotronics-Noromed, Inc.Kent, WA, United StatesManufacturer, Repackager or relabeler2July 20, 2004000api.fda.gov
BTL Industries JSCPlovdiv, BulgariaManufacturer1May 9, 2025000api.fda.gov
Ito Co., Ltd.Kawaguchi Saitama, JapanSpecification developer1May 5, 2021000api.fda.gov
ITO CO., LTD. Tsukuba FactoryInashiki-Gun Ibaraki, JapanManufacturer1May 5, 2021000api.fda.gov

Updated May 9, 2025. 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.