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Data / Medical devices / Device, Mixing And Weighing, Semi-Automated

Device, Mixing And Weighing, Semi-Automated (MYJ): 4 FDA-registered makers in 3 countries

4 establishments in 3 countries are registered with the FDA to make Device, Mixing And Weighing, Semi-Automated (product code MYJ, Class 2, 21 CFR 864.9195). 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.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Product code
MYJ
Device class
2
Regulation
864.9195
Medical specialty
Hematology

Makers by country

CountryMakers
France2
Sweden1
Italy1

Makers of Device, Mixing And Weighing, Semi-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
AB Elektronik-Konstruktion Innovation (Abelko)Lulea, SwedenManufacturer0000api.fda.gov
Delcon SRLGrassobbio Bergamo, ItalyManufacturer0000api.fda.gov
Maco PharmaMOUVAUX Hauts-de-France, FranceComplaint file establishment, Exporter to the US, Specification developer0000api.fda.gov
Macoproductions S.A.S.TOURCOING Nord, FranceManufacturer0000api.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.