Data / Medical devices / Accelerator, Linear, Medical

Accelerator, Linear, Medical (IYE): 97 FDA-registered makers in 20 countries

97 establishments in 20 countries are registered with the FDA to make Accelerator, Linear, Medical (product code IYE, Class 2, 21 CFR 892.5050). 78 of them have a 510(k) clearance or PMA approval on file and 20 have a recall event. The FDA has issued 738 510(k) clearances under this code, the latest on September 16, 2026, and lists 357 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

IYE

Device class

2

Regulation

892.5050

Medical specialty

Radiology

Makers by country

Makers of Accelerator, Linear, Medical

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 September 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.