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Data / Medical devices / Washer Of Body Waste Receptacles

Washer Of Body Waste Receptacles (FLH): 19 FDA-registered makers in 7 countries

19 establishments in 7 countries are registered with the FDA to make Washer Of Body Waste Receptacles (product code FLH, Class 1, 21 CFR 880.6800). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
FLH
Device class
1
Regulation
880.6800
Medical specialty
General Hospital

Makers by country

CountryMakers
China12
United States2
Poland1
Germany1
Italy1
Canada1
United Kingdom1

Makers of Washer Of Body Waste Receptacles

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
Ari Medical Technology Co., Ltd.Hefei Anhui, ChinaManufacturer0000api.fda.gov
ArjoHuntleigh Polska Sp. zo.o.Poznan Wielkopolskie, PolandComplaint file establishment, Manufacturer0000api.fda.gov
Guangzhou Amk Medical Equipment Co.,ltd.Guang zhou Guangdong, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Guangzhou Nuoning Medical Supplies Co.,ltdGuangzhou Guangdong, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Hefei MT Medical Co.,ltd.Hefei Anhui, ChinaExporter to the US, Manufacturer0000api.fda.gov
Infitek Co., Ltd.Shanghai, ChinaManufacturer0000api.fda.gov
Jiangsu Rooe Medical Technology Co., Ltd.Zhangjiagang City Jiangsu, ChinaExporter to the US, Manufacturer0000api.fda.gov
Jiangsu Saikang Medical Equipment Co., LtdZhangjiagang Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Jiangsu Yongfa Medical Equipment Technology Co., LtdZhangjiagang City Jiangsu, ChinaManufacturer0000api.fda.gov
Labpeak Co.,ltdJinan Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov
M D Technologies, Inc.Elizabeth, IL, United StatesManufacturer0000api.fda.gov
Meiko Maschinenbau GMBH & Co. KGOFFENBURG Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
Saferlife Products Co.,ltd.Guangzhou Guangdong, ChinaContract manufacturer0000api.fda.gov
Scitek Global Co.,ltdJinan Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Shanghai No. 2 Medical College Duhang Medical Equipment FactoryShanghai, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Steelco S.P.A.Riese Pio X Treviso, ItalyComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Vernacare Canada, Inc.Maple Ontario, CanadaSpecification developer0000api.fda.gov
Vernacare Ltd.Bolton Lancashire, United KingdomManufacturer0000api.fda.gov
Zimmer Surgical, Inc.Dover, OH, United StatesManufacturer0000api.fda.gov

Updated November 2, 2026. 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.