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Data / Medical devices / Table, Examination, Medical, Powered / United States

FDA-registered makers of Table, Examination, Medical, Powered in the United States: 11 establishments

11 establishments in the United States are registered with the FDA to make Table, Examination, Medical, Powered (product code LGX). 0 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Table, Examination, Medical, Powered
Product code
LGX
Country
United States

Makers of Table, Examination, Medical, Powered in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Dexta Corp.Napa, CA, United StatesManufacturer0000api.fda.gov
Durabuilt Medical Corp.Texarkana, AR, United StatesManufacturer0000api.fda.gov
Heritage Medical Products, incWest Plains, MO, United StatesManufacturer0010api.fda.gov
Intensa, Inc.High Point, NC, United StatesManufacturer0000api.fda.gov
Leander, LLCLawrence, KS, United StatesManufacturer0000api.fda.gov
Marketlab IncorporatedCaledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Med-Mizer, IncBatesville, IN, United StatesManufacturer0000api.fda.gov
Medical Positioning, Inc.Lenexa, KS, United StatesManufacturer0020api.fda.gov
Oakworks, Inc.New Freedom, PA, United StatesManufacturer0020api.fda.gov
Stille Surgical Inc.Lombard, IL, United StatesContract manufacturer0000api.fda.gov
The Brewer Company LLCMenomonee Falls, WI, United StatesManufacturer0010api.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.