Data / Medical devices / System, X-Ray, Tomography, Computed

System, X-Ray, Tomography, Computed (JAK): 113 FDA-registered makers in 21 countries

113 establishments in 21 countries are registered with the FDA to make System, X-Ray, Tomography, Computed (product code JAK, Class 2, 21 CFR 892.1750). 69 of them have a 510(k) clearance or PMA approval on file and 17 have a recall event. The FDA has issued 827 510(k) clearances under this code, the latest on October 16, 2026, and lists 375 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

JAK

Device class

2

Regulation

892.1750

Medical specialty

Radiology

Makers by country

Makers of System, X-Ray, Tomography, Computed

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.

Updated October 16, 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.