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Data / Medical devices / United States / Pride Mobility Products Corp.

Pride Mobility Products Corp.: FDA-registered device maker in Duryea, PA, United States, 26 510(k) clearances

Pride Mobility Products Corp. is registered with the FDA (registration 2531465) in Duryea, PA, United States. It lists 25 device types. The FDA files 26 510(k) clearances under its listings, the newest dated May 12, 2022. 6 recall events name it as the recalling firm. Registered through 2026. FDA data exported November 2, 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
2531465
FEI number
3005068474
Address
401 York Ave., Duryea, PA, United States, 18642
Owner or operator
PRIDE MOBILITY PRODUCTS CORP. (2523375)
Roles
Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer
First device listed
June 23, 1988
Registered through
2026
Brand names listed
ACCESSORIES, WHEELCHAIR, ARMBOARD, WHEELCHAIR, ARMREST, WHEELCHAIR, BELT, WHEELCHAIR, BOARD, LAP, WHEELCHAIR, BOARD, SCOOTER, PRONE, BRAKE, EXTENSION, WHEELCHAIR, CHAIR, WITH CASTERS and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, WheelchairKNO1Manufactureraccessdata.fda.gov
Armboard, WheelchairIMY1Manufactureraccessdata.fda.gov
Armrest, WheelchairIML1Manufactureraccessdata.fda.gov
Belt, WheelchairIQB1Manufactureraccessdata.fda.gov
Board, Lap, WheelchairIMX1Manufactureraccessdata.fda.gov
Board, Scooter, ProneKNL1Manufactureraccessdata.fda.gov
Brake, Extension, WheelchairIMW1Manufactureraccessdata.fda.gov
Chair, Adjustable, MechanicalINN1Manufactureraccessdata.fda.gov
Chair, Positioning, ElectricINO2Manufacturer, Specification developeraccessdata.fda.gov
Chair, With CastersINM1Manufactureraccessdata.fda.gov
Climber, Curb, WheelchairIMN1Manufactureraccessdata.fda.gov
Components, WheelchairKNN1Manufactureraccessdata.fda.gov
Cuff, Pusher, WheelchairINC1Manufactureraccessdata.fda.gov
Cushion, WheelchairIMP1Manufacturer, Repackager or relabeler, Specification developeraccessdata.fda.gov
Device, Anti-Tip, WheelchairIMR1Manufactureraccessdata.fda.gov
Footrest, WheelchairIMM1Manufactureraccessdata.fda.gov
Handrim, WheelchairIMO1Manufactureraccessdata.fda.gov
Hill Holder, WheelchairINA1Manufactureraccessdata.fda.gov
Holder, Crutch And Cane, WheelchairIMZ1Manufactureraccessdata.fda.gov
Lift, Patient, Non-Ac-PoweredFSA1Complaint file establishmentaccessdata.fda.gov
Restraint, Wheelchair, Non-ProtectiveKID1Manufactureraccessdata.fda.gov
Support, Head And Trunk, WheelchairIMS1Manufactureraccessdata.fda.gov
Vehicle, Motorized 3-WheeledINI2Manufactureraccessdata.fda.gov
Wheelchair, MechanicalIOR1Manufactureraccessdata.fda.gov
Wheelchair, PoweredITI2Manufactureraccessdata.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
May 12, 2022K220747Power Wheelchair (N5515B)ITISubstantially EquivalentZhejiang Innuovo Rehabilitation Devices Co.,Ltdaccessdata.fda.gov
July 23, 2015K143383Q6 Edge EMITISubstantially EquivalentPride Mobility Product Corporationaccessdata.fda.gov
April 18, 2012K113488JAZZY ELITE 6ITISubstantially EquivalentPride Mobility Product Corporrationaccessdata.fda.gov
February 29, 2012K112815QUANTUM BARIATRIC 451ITISubstantially EquivalentPride Mobility Product Corporrationaccessdata.fda.gov
August 12, 2011K111739KIDS ROCK 3 CHAIRIORSubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
December 2, 2009K091578LIFT CHAIR, MODEL T3INOSubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
October 23, 2009K092961JAZZY FRONTIEITISubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
July 16, 2009K092088VICTORY XL 130 FOUR WHEEL SCOOTER, MODEL SC713INISubstantially 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
March 19, 2009K090524GO GO ELITE TRAVELER V THREE WHEEL SCOOTER, MODEL SC40EVINISubstantially 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
September 12, 2006K062160GO GO MINI, MODEL SC30INISubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
September 9, 2005K052353Z-CHAIRITISubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
October 21, 2004K042444LITESTREAM 500EIORSubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
October 6, 2004K042612JAZZY 600ITISubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
September 8, 2004K041346SYNERGY ULTIMATEITISubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
July 13, 2001K011993QUANTUM BLASTITISubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
September 26, 2000K001970JET 1 POWERED WHEELCHAIRITISubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
September 8, 1995K953342TMR48INOSubstantially EquivalentPride Health Care, Inc.accessdata.fda.gov
November 7, 1994K944939CELEBRITY XL SC445INISubstantially EquivalentPride Health Care, Inc.accessdata.fda.gov
March 28, 1994K930953CELEBRITY SC440INISubstantially Equivalent for Some IndicationsPride Health Care, Inc.accessdata.fda.gov
March 28, 1994K926296CELEBRITY SC400INISubstantially Equivalent for Some IndicationsPride Health Care, Inc.accessdata.fda.gov
July 22, 1993K931349TMR-670INOSubstantially EquivalentPride Health Care, Inc.accessdata.fda.gov

Recalls

Recall events where this establishment is the recalling firm, matched on its FEI.

InitiatedEventClassStatusProductReasonSource
June 25, 202699286Class IIOngoingBrand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum 4Front 2 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), Component: ControllerIf the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain accessdata.fda.gov
December 1, 201675881Class IITerminatedTRU-Balance 3 Power Positioning Systems, TB3 Lift/Tilt/Recline (Gen 1). Mobility Medical DeviceThe interface between the TB3 back and tilt base can separate when tilted beyond the specified angle.accessdata.fda.gov
June 22, 201159438Not yet classifiedTerminatedVictory 10, 3 Wheel (SC610) Mobility medical deviceContract manufacturer error. Component part(s) (fuses) specifications were not adhered to as outlined in Pride's Engineering drawings.accessdata.fda.gov
November 26, 201057350Class IITerminatedVictory 9 with Power Seat (SC609PS) Motorized wheelchair with elevating seat.The main harness connector was manufactured without the required back shield sealing protection. As a result, there is the potential for water to seep through the nonconforming harness.accessdata.fda.gov
February 1, 201054617Not yet classifiedTerminatedJazzy Select with XLR Port HarnessImproper set-up of the wire harness can allow wires to be pulled from their intended position and become caught under the motor mounting bracket located under the powered wheelchair. This can cause the wire connector and/or the wire itself to be pulled or pinched which can lead to a short or open circuit.accessdata.fda.gov
April 11, 200847807Not yet classifiedTerminatedQ-Logic Controller Software used on the following power wheelchairs: Q6000, Q6000XL, Q6000Z, R4000, Q600, Q600XL, Q610, Q1107, Q600E, and Dynamo 1107Software - Watch dog timer feature was disabled.accessdata.fda.gov

Compare with other makers

Updated July 31, 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.