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Data / Medical devices / United States / Empowerride LLC

Empowerride LLC: FDA-registered device maker in Elkhorn, NE, United States, 1 510(k) clearance

Empowerride LLC is registered with the FDA (registration 3043237012) in Elkhorn, NE, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 12, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3043237012
Address
18874 Patrick Ave, Elkhorn, NE, United States, 68022
Owner or operator
EmpowerRide LLC (10095223)
Roles
Complaint file establishment, Specification developer
First device listed
February 6, 2026
Registered through
2026
Brand names listed
Navigator

Devices it lists

DeviceProduct codeClassRoleSource
Stroller, AdaptiveLBE1Complaint file establishment, Specification developeraccessdata.fda.gov
Wheelchair, MechanicalIOR1Complaint file establishment, Specification developeraccessdata.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
January 12, 2026K251886EmpowerRide NAVIGATORIORSubstantially EquivalentEmpower Ride, LLCaccessdata.fda.gov

Compare with other makers

Updated January 12, 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.