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Data / Medical devices / Scale, Sponge, Surgical, Electrically-Powered

Scale, Sponge, Surgical, Electrically-Powered (MRL): 9 FDA-registered makers in 6 countries

9 establishments in 6 countries are registered with the FDA to make Scale, Sponge, Surgical, Electrically-Powered (product code MRL, 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 26, 1997, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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

Makers by country

CountryMakers
United States4
Mexico1
India1
Canada1
China1
Taiwan1

Makers of Scale, Sponge, Surgical, Electrically-Powered

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
Acaia Corp.Alhambra, CA, United StatesContract manufacturer0000api.fda.gov
Cardinal Scale MFG. Co.Webb City, MO, United StatesManufacturer0000api.fda.gov
Fabricantes De Basculas Torrey SA De CVMONTERREY Nuevo Leon, MexicoContract manufacturer0000api.fda.gov
Greens Surgicals Private LimitedVadodara Gujarat, IndiaManufacturer0000api.fda.gov
Hygie Canada Inc.Drummondville Quebec, CanadaExporter to the US, Manufacturer, Specification developer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Nanjing Easthigh Measurement Co LtdNanjing Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Snowrex International Co., Ltd.Taipei, TaiwanContract manufacturer0000api.fda.gov
Stryker InstrumentsPortage, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov

Updated February 26, 1997. 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.