Data / Medical devices / Vibrator For Therapeutic Use, Genital

Vibrator For Therapeutic Use, Genital (KXQ): 31 FDA-registered makers in 10 countries

31 establishments in 10 countries are registered with the FDA to make Vibrator For Therapeutic Use, Genital (product code KXQ, Class 2, 21 CFR 884.5960). 0 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 3, 2014, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

KXQ

Device class

2

Regulation

884.5960

Medical specialty

Obstetrics/Gynecology

Makers by country

Makers of Vibrator For Therapeutic Use, Genital

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 October 3, 2014. 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.