Skip to the page

Data / Medical devices / United States / Free Wheelchair Mission

Free Wheelchair Mission: FDA-registered device maker in Irvine, CA, United States, 3 510(k) clearances

Free Wheelchair Mission is registered with the FDA (registration 3009235796) in Irvine, CA, United States. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated July 24, 2026. Registered through 2027. FDA data exported November 3, 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.

FDA registration number
3009235796
Address
15279 Alton Pkwy Ste 300, Irvine, CA, United States, 92618
Owner or operator
Free Wheelchair Mission (10041035)
Roles
Complaint file establishment, Specification developer
First device listed
June 13, 2012
Registered through
2027
Brand names listed
GEN 4 JOY Wheelchair, GEN_3 Mechanical Wheelchair, Wheelchair, mechanical

Devices it lists

DeviceProduct codeClassRoleSource
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
July 24, 2026K252370GEN 4 JOY WheelchairIORSubstantially EquivalentFree Wheelchair Missionaccessdata.fda.gov
December 17, 2014K141691GEN_3IORSubstantially EquivalentFree Wheelchair Missionaccessdata.fda.gov
May 7, 2012K113713GEN_2 MECHANICAL WHEELCHAIRIORSubstantially EquivalentFree Wheelchair Missionaccessdata.fda.gov

Compare with other makers

Updated July 24, 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.