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Data / Medical devices / Hemorrhoid Prevention Pressure Wedge

Hemorrhoid Prevention Pressure Wedge (OOA): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Hemorrhoid Prevention Pressure Wedge (product code OOA, Class 2, 21 CFR 884.5200). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on January 13, 2011, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
OOA
Device class
2
Regulation
884.5200
Medical specialty
Obstetrics/Gynecology

Makers by country

CountryMakers
China2
United States1

Makers of Hemorrhoid Prevention Pressure Wedge

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
Dong Guan Jia Shuan Industrial Co., LtdDongguan Guangdong, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Picard Healthcare Technology (Dongguan) Co. LtdDongguan Guangdong, ChinaManufacturer0000api.fda.gov
Stetrix Inc.Memphis, TN, United StatesManufacturer0000api.fda.gov

Updated January 13, 2011. 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.