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Data / Medical devices / Table, Radiographic, Stationary Top / United States

FDA-registered makers of Table, Radiographic, Stationary Top in the United States: 8 establishments

8 establishments in the United States are registered with the FDA to make Table, Radiographic, Stationary Top (product code IXQ). 2 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.

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Device
Table, Radiographic, Stationary Top
Product code
IXQ
Country
United States

Makers of Table, Radiographic, Stationary Top in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Anholt Technologies Inc.Avondale, PA, United StatesManufacturer1December 5, 1997000api.fda.gov
Medtec LLCOrange City, IA, United StatesManufacturer1December 5, 1997020api.fda.gov
Accogent PauschEatontown, NJ, United StatesManufacturer0000api.fda.gov
Core Labs, LLC.Englewood, CO, United StatesManufacturer0000api.fda.gov
Diacor, Inc.Mount Pleasant, UT, United StatesManufacturer0000api.fda.gov
Oakworks, Inc.New Freedom, PA, United StatesManufacturer0000api.fda.gov
Radiation Products Design, Inc.Albertville, MN, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Summit Industries, LLCNiles, IL, United StatesComplaint file establishment, Manufacturer0000api.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.