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Data / Medical devices / Grinder, Tissue

Grinder, Tissue (LEC): 5 FDA-registered makers in 3 countries

5 establishments in 3 countries are registered with the FDA to make Grinder, Tissue (product code LEC, Class 1, 21 CFR 864.3010). 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
LEC
Device class
1
Regulation
864.3010
Medical specialty
Pathology

Makers by country

CountryMakers
China2
South Korea2
United States1

Makers of Grinder, Tissue

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
Biomedical Polymers, Inc.Sterling, MA, United StatesManufacturer0000api.fda.gov
Guangzhou Four E's Scientific Co., Ltd.GUANGZHOU Guangdong, ChinaRepackager or relabeler, Specification developer0000api.fda.gov
MBD Co., Ltd.Suwon-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
MEDIKAN CO., Ltd.Gangseo-gu Seoul, South KoreaManufacturer0000api.fda.gov
Qibei Technology Co., LimitedKL Hong Kong, ChinaExporter to the US, Manufacturer0000api.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.