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Data / Medical devices / Scrapper, Skin Specimen

Scrapper, Skin Specimen (LXK): 9 FDA-registered makers in 3 countries

9 establishments in 3 countries are registered with the FDA to make Scrapper, Skin Specimen (product code LXK, Class 1, 21 CFR 878.4800). 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 April 6, 1988, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
LXK
Device class
1
Regulation
878.4800
Medical specialty
General, Plastic Surgery

Makers by country

CountryMakers
China4
Pakistan3
Germany2

Makers of Scrapper, Skin Specimen

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
Aesculap AGTUTTLINGEN, DONAU Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
Bauer Und Haselbarth-Chirurg GMBHELLERAU Schleswig-Holstein, GermanyContract manufacturer0000api.fda.gov
Foshan Ruiyi Electronic Technology Co., Ltd.Foshan Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Falcon Surgical Co. (Pvt.) Ltd.Sialkot Punjab, PakistanManufacturer0000api.fda.gov
Hive International Pvt Ltd.Sialkot Punjab, PakistanManufacturer0000api.fda.gov
Miley Technology (hebei) Co., LtdHandan Hebei, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Shanghai Reach Medical Instrument Co., LtdShanghai, ChinaManufacturer0000api.fda.gov
Shenzhen Trendz Technology Co.,ltdShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Surgicon Pvt LtdSialkot Punjab, PakistanManufacturer0000api.fda.gov

Updated April 6, 1988. 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.