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Data / Medical devices / United States / Pride Mobility Products Corporation

Pride Mobility Products Corporation: FDA-registered device maker in Pontotoc, MS, United States, 7 510(k) clearances

Pride Mobility Products Corporation is registered with the FDA (registration 3012425482) in Pontotoc, MS, United States. It lists 3 device types. The FDA files 7 510(k) clearances under its listings, the newest dated May 12, 2022. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3012425482
Address
380 Maggie Dr, Pontotoc, MS, United States, 38863
Owner or operator
PRIDE MOBILITY PRODUCTS CORP. (2523375)
Roles
Manufacturer
First device listed
April 22, 2008
Registered through
2026
Brand names listed
Victory HD (SC710HD)

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
May 12, 2022K220747Power Wheelchair (N5515B)ITISubstantially EquivalentZhejiang Innuovo Rehabilitation Devices Co.,Ltdaccessdata.fda.gov
December 2, 2009K091578LIFT CHAIR, MODEL T3INOSubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
May 11, 2009K091113MAXIMA V, THREE WHEEL SCOOTER, MODEL SC900V MAXIMA V, FOUR WHEEL SCOOTER, MODEL SC940VINISubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
August 17, 2007K072165VICTORY THREE WHEEL SCOOTER, MODEL: SC610INISubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
August 1, 2007K071949VICTORY, 4 WHEEL SCOOTER / MODEL, # SC1740INISubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
April 16, 2007K070950LIFT CHAIR, MODEL C5INOSubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
November 17, 2006K063389GO GO ELITE TRAVELLER PLUS 4 WHEEL SCOOTER, MODEL SC54INISubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov

Compare with other makers

Updated May 12, 2022. 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.