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Data / Medical devices / Device, Finger-Sucking

Device, Finger-Sucking (LQX): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Device, Finger-Sucking (product code LQX, Class 1, 21 CFR 890.3475). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on March 23, 1995, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
LQX
Device class
1
Regulation
890.3475
Medical specialty
Physical Medicine

Makers by country

CountryMakers
China2
United States1

Makers of Device, Finger-Sucking

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
Med Et Al Development Corp.Matthews, NC, United StatesManufacturer1March 23, 1995000api.fda.gov
Changzhou Meiguan Care Products Technology Co.,ltd.Changzhou Jiangsu, ChinaExporter to the US, Manufacturer0000api.fda.gov
Gauke (hubei) Healthcare Co., LtdHuanggang City Hubei, ChinaManufacturer, Repackager or relabeler0000api.fda.gov

Updated March 23, 1995. 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.