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Data / Medical devices / Insulin Pump Secondary Display / United States

FDA-registered makers of Insulin Pump Secondary Display in the United States: 6 establishments

6 establishments in the United States are registered with the FDA to make Insulin Pump Secondary Display (product code PKU). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Insulin Pump Secondary Display
Product code
PKU
Country
United States

Makers of Insulin Pump Secondary Display in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Beta Bionics, Inc.Irvine, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Deka Research & Development Corp.Manchester, NH, United StatesSpecification developer0000api.fda.gov
Intricon CorporationArden Hills, MN, United StatesManufacturer0000api.fda.gov
Medtronic MinimedNorthridge, CA, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Millyard Advanced Medical Products LLCManchester, NH, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Tandem Diabetes Care, Inc.San Diego, CA, United StatesManufacturer0000api.fda.gov

Updated November 3, 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.