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Data / Medical devices / United States / Williams Healthcare Systems, LLC.

Williams Healthcare Systems, LLC.: FDA-registered device maker in Elgin, IL, United States, 5 510(k) clearances

Williams Healthcare Systems, LLC. is registered with the FDA (registration 1415746) in Elgin, IL, United States. It lists 3 device types. The FDA files 5 510(k) clearances under its listings, the newest dated February 2, 1994. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1415746
Address
158 N.edison Ave., Elgin, IL, United States, 60123
Owner or operator
Foundational Williams LLC (10092599)
Roles
Manufacturer
First device listed
January 24, 2025
Registered through
2026
Brand names listed
Combi 2.5 Intersegmental traction table, WILLIAMS ADVANTAGE ELEVATION TABLE, ZENITH COX FLEXION CHIROPRACTIC TABLE, ZENITH HYLO AND VERTI-LIFT CHIROPRACTIC TABLES, ZENITH TRAVELER CHIROPRACTIC TABLE

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
February 2, 1994K933443COMBI 2.5 INTERSEGMENTAL TRACTION TABLEJFBSubstantially EquivalentWilliams Healthcare Systems, LLCaccessdata.fda.gov
August 7, 1992K922719WILLIAMS ADVANTAGE ELEVATION TABLEINQSubstantially EquivalentWilliams Manufacturing Co.accessdata.fda.gov
January 18, 1991K905685ZENITH COX FLEXION CHIROPRACTIC TABLEINQSubstantially EquivalentWilliams Manufacturing Co.accessdata.fda.gov
July 26, 1990K902971ZENITH HYLO AND VERTI-LIFT CHIROPRACTIC TABLESINQSubstantially EquivalentWilliams Manufacturing Co.accessdata.fda.gov
February 3, 1988K880222ZENITH TRAVELER CHIROPRACTIC TABLEINWSubstantially EquivalentWilliams Manufacturing Co.accessdata.fda.gov

Compare with other makers

Updated February 2, 1994. 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.