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Data / Medical devices / Scale, Surgical Sponge

Scale, Surgical Sponge (FQA): 11 FDA-registered makers in 4 countries

11 establishments in 4 countries are registered with the FDA to make Scale, Surgical Sponge (product code FQA, Class 1, 21 CFR 880.2740). 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 February 28, 1983, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

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Product code
FQA
Device class
1
Regulation
880.2740
Medical specialty
General Hospital

Makers by country

CountryMakers
United States4
China4
India2
Germany1

Makers of Scale, Surgical Sponge

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
Cardinal Scale MFG. Co.Webb City, MO, United StatesManufacturer0000api.fda.gov
Changzhou Recoo Healthcare Co., Ltd.Changzhou Jiangsu, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Doran Scales, Inc.Saint Charles, IL, United StatesManufacturer, Specification developer0000api.fda.gov
Dongguan Beaver Plastic & Metal Products Co., Ltd.Dongguan City Guangdong, ChinaContract manufacturer0000api.fda.gov
Greens Surgicals Private LimitedVadodara Gujarat, IndiaManufacturer0000api.fda.gov
Gesco Healthcare Private LimitedCHENNAI, Tamil Nadu, IndiaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
SecaHamburg, GermanyManufacturer0000api.fda.gov
SR Instruments, Inc.Tonawanda, NY, United StatesManufacturer, Specification developer0000api.fda.gov
Xodus Medical, Inc.New Kensington, PA, United StatesManufacturer0000api.fda.gov
Zhejiang Shuyou Surgical Instrument Co., LtdHuzhou Zhejiang, ChinaContract manufacturer0000api.fda.gov
seca Medical Measuring Systems (pinghu) co. ltd.Pinghu Zhejiang, ChinaContract manufacturer0000api.fda.gov

Updated February 28, 1983. 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.