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Data / Medical devices / United States / Bruno Independent Living Aids, Inc.

Bruno Independent Living Aids, Inc.: FDA-registered device maker in Oconomowoc, WI, United States, 1 510(k) clearance

Bruno Independent Living Aids, Inc. is registered with the FDA (registration 2131358) in Oconomowoc, WI, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 10, 2000. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2131358
FEI number
1000116427
Address
1780 Executive DR., Oconomowoc, WI, United States, 53066
Owner or operator
BRUNO INDEPENDENT LIVING AIDS, INC. (9005397)
Roles
Manufacturer, Repackager or relabeler
First device listed
January 2, 2008
Registered through
2026
Brand names listed
Vertical Platform Lift, Wheelchair, mechanical

Devices it lists

DeviceProduct codeClassRoleSource
Permanently Mounted Wheelchair Platform LiftPCE2Manufactureraccessdata.fda.gov
Wheelchair, MechanicalIOR1Repackager or relabeleraccessdata.fda.gov

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
August 10, 2000K002205CARONYIORSubstantially EquivalentBruno Independent Living Aids, Inc.accessdata.fda.gov

Compare with other makers

Updated August 10, 2000. 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.