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Data / Medical devices / Table, Powered / United States

FDA-registered makers of Table, Powered in the United States: 15 establishments

15 establishments in the United States are registered with the FDA to make Table, Powered (product code INQ). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Table, Powered
Product code
INQ
Country
United States

Makers of Table, Powered in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Hill LaboratoriesFrazer, PA, United StatesManufacturer9July 6, 1995000api.fda.gov
Williams Healthcare Systems, LLC.Elgin, IL, United StatesManufacturer3August 7, 1992000api.fda.gov
Altimate Medical, Inc.Morton, MN, United StatesManufacturer0000api.fda.gov
Armedica MFG.Greenwood, AR, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Clinton Industries, IncYork, PA, United StatesManufacturer0000api.fda.gov
Djo, LLCCarlsbad, CA, United StatesSpecification developer0000api.fda.gov
Fresh Water Tables LLCGrand Rapids, MI, United StatesManufacturer0000api.fda.gov
Hausmann Enterprises, LLCNorthvale, NJ, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Haven Medical, LLCGrand Haven, MI, United StatesManufacturer0000api.fda.gov
North Coast Medical, Inc.Morgan Hill, CA, United StatesManufacturer0000api.fda.gov
Pivotal Health SolutionsWatertown, SD, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Radiation Products Design, Inc.Albertville, MN, United StatesManufacturer0000api.fda.gov
Tri W-G, Inc.Valley City, ND, United StatesManufacturer0000api.fda.gov
Trumedical Solutions, LLC.Ooltewah, TN, United StatesContract manufacturer, Manufacturer0000api.fda.gov
United Metal Fabricators, Inc.Johnstown, PA, United StatesManufacturer0000api.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.