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Data / Medical devices / Canada / Future Mobility Healthcare Inc.

Future Mobility Healthcare Inc.: FDA-registered device maker in MISSISSAUGA Ontario, Canada, 6 510(k) clearances

Future Mobility Healthcare Inc. is registered with the FDA (registration 3004577612) in MISSISSAUGA Ontario, Canada. It lists 13 device types. The FDA files 6 510(k) clearances under its listings, the newest dated December 5, 2013. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3004577612
Address
6750 Professional Court, MISSISSAUGA Ontario, Canada, L4V 1X6
Owner or operator
FUTURE MOBILITY HEALTHCARE INC. (9079483)
Roles
Manufacturer
First device listed
November 10, 2005
Registered through
2026
Brand names listed
ACCESSORIES WHEELCHAIRS, ARMREST FOR WHEELCHAIR. VARIOUS TYPES, BACKRESTS-AIR BACK, BASIC BACK, LUNAR BACK, LUNAR HD BACK, BELTS AND CHEST STRAPS, CAPELLA, COMMODE CHAIR, SHOWER, SELF PROPELLED AND ATTENDANT, COMPONENTS, FOOTREST, WHEELCHAIR and more

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
December 5, 2013K130788CAPELLAIORSubstantially EquivalentFuture Mobility Healthcare, Inc.accessdata.fda.gov
January 3, 2011K103073SUPER CHAIR FOR KIDS BY ORIONIORSubstantially EquivalentFuture Mobility Healthcare, Inc.accessdata.fda.gov
October 20, 2010K102031GALAXY LITEIORSubstantially EquivalentFuture Mobility Healthcare, Inc.accessdata.fda.gov
June 4, 2010K101277ORION II (HEAVY DUTY 350 LBS AND 500 LBS)IORSubstantially EquivalentFuture Mobility Healthcare, Inc.accessdata.fda.gov
May 23, 2006K061010FUTURE MOBILITY HEALTHCARE INC. ORION II WHEELCHAIR AND STELLATO MECHANICAL WHEELCHAIRIORSubstantially EquivalentFuture Mobility Healthcare, Inc.accessdata.fda.gov
March 20, 1995K951138MODELS PHOENIX AND CONCEPT 45 MANUAL MECHANICAL WHEELCHAIRSIORSubstantially EquivalentInvacare Corp.accessdata.fda.gov

Compare with other makers

Updated December 5, 2013. 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.