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Data / Medical devices / Spinner, Slide, Automated

Spinner, Slide, Automated (GKJ): 4 FDA-registered makers in 4 countries

4 establishments in 4 countries are registered with the FDA to make Spinner, Slide, Automated (product code GKJ, Class 1, 21 CFR 864.5850). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 6 510(k) clearances under this code, the latest on December 23, 1985, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

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Product code
GKJ
Device class
1
Regulation
864.5850
Medical specialty
Hematology

Makers by country

CountryMakers
Germany1
United States1
Australia1
France1

Makers of Spinner, Slide, Automated

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
Bio-Gram Diagnostics GMBHWorms Rhineland-Palatinate, GermanyManufacturer, Specification developer0000api.fda.gov
J.P. Gilbert Co.Boyertown, PA, United StatesManufacturer0000api.fda.gov
Leica Biosystems Melbourne Pty LtdMELBOURNE Victoria, AustraliaContract manufacturer0000api.fda.gov
Ral DiagnosticsMartillac Gironde, FranceManufacturer0000api.fda.gov

Updated December 23, 1985. 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.