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.
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- 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
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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 12, 2022 | K220747 | Power Wheelchair (N5515B) | ITI | Substantially Equivalent | Zhejiang Innuovo Rehabilitation Devices Co.,Ltd | accessdata.fda.gov |
| July 23, 2015 | K143383 | Q6 Edge EM | ITI | Substantially Equivalent | Pride Mobility Product Corporation | accessdata.fda.gov |
| April 18, 2012 | K113488 | JAZZY ELITE 6 | ITI | Substantially Equivalent | Pride Mobility Product Corporration | accessdata.fda.gov |
| February 29, 2012 | K112815 | QUANTUM BARIATRIC 451 | ITI | Substantially Equivalent | Pride Mobility Product Corporration | accessdata.fda.gov |
| August 12, 2011 | K111739 | KIDS ROCK 3 CHAIR | IOR | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| December 2, 2009 | K091578 | LIFT CHAIR, MODEL T3 | INO | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| October 23, 2009 | K092961 | JAZZY FRONTIE | ITI | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| July 16, 2009 | K092088 | VICTORY XL 130 FOUR WHEEL SCOOTER, MODEL SC713 | INI | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| May 11, 2009 | K091113 | MAXIMA V, THREE WHEEL SCOOTER, MODEL SC900V MAXIMA V, FOUR WHEEL SCOOTER, MODEL SC940V | INI | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| March 19, 2009 | K090524 | GO GO ELITE TRAVELER V THREE WHEEL SCOOTER, MODEL SC40EV | INI | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| August 17, 2007 | K072165 | VICTORY THREE WHEEL SCOOTER, MODEL: SC610 | INI | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| August 1, 2007 | K071949 | VICTORY, 4 WHEEL SCOOTER / MODEL, # SC1740 | INI | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| April 16, 2007 | K070950 | LIFT CHAIR, MODEL C5 | INO | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| November 17, 2006 | K063389 | GO GO ELITE TRAVELLER PLUS 4 WHEEL SCOOTER, MODEL SC54 | INI | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| September 12, 2006 | K062160 | GO GO MINI, MODEL SC30 | INI | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| September 9, 2005 | K052353 | Z-CHAIR | ITI | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| October 21, 2004 | K042444 | LITESTREAM 500E | IOR | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| October 6, 2004 | K042612 | JAZZY 600 | ITI | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| September 8, 2004 | K041346 | SYNERGY ULTIMATE | ITI | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| July 13, 2001 | K011993 | QUANTUM BLAST | ITI | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| September 26, 2000 | K001970 | JET 1 POWERED WHEELCHAIR | ITI | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| September 8, 1995 | K953342 | TMR48 | INO | Substantially Equivalent | Pride Health Care, Inc. | accessdata.fda.gov |
| November 7, 1994 | K944939 | CELEBRITY XL SC445 | INI | Substantially Equivalent | Pride Health Care, Inc. | accessdata.fda.gov |
| March 28, 1994 | K930953 | CELEBRITY SC440 | INI | Substantially Equivalent for Some Indications | Pride Health Care, Inc. | accessdata.fda.gov |
| March 28, 1994 | K926296 | CELEBRITY SC400 | INI | Substantially Equivalent for Some Indications | Pride Health Care, Inc. | accessdata.fda.gov |
| July 22, 1993 | K931349 | TMR-670 | INO | Substantially Equivalent | Pride Health Care, Inc. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| June 25, 2026 | 99286 | Class II | Ongoing | Brand 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: Controller | If 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, 2016 | 75881 | Class II | Terminated | TRU-Balance 3 Power Positioning Systems, TB3 Lift/Tilt/Recline (Gen 1). Mobility Medical Device | The interface between the TB3 back and tilt base can separate when tilted beyond the specified angle. | accessdata.fda.gov |
| June 22, 2011 | 59438 | Not yet classified | Terminated | Victory 10, 3 Wheel (SC610) Mobility medical device | Contract manufacturer error. Component part(s) (fuses) specifications were not adhered to as outlined in Pride's Engineering drawings. | accessdata.fda.gov |
| November 26, 2010 | 57350 | Class II | Terminated | Victory 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, 2010 | 54617 | Not yet classified | Terminated | Jazzy Select with XLR Port Harness | Improper 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, 2008 | 47807 | Not yet classified | Terminated | Q-Logic Controller Software used on the following power wheelchairs: Q6000, Q6000XL, Q6000Z, R4000, Q600, Q600XL, Q610, Q1107, Q600E, and Dynamo 1107 | Software - Watch dog timer feature was disabled. | accessdata.fda.gov |
Compare with other makers
- All makers of Vehicle, Motorized 3-Wheeled
- All makers of Brake, Extension, Wheelchair
- All makers of Device, Anti-Tip, Wheelchair
- All makers of Chair, Positioning, Electric
- All makers of Accessories, Wheelchair
- All makers of Footrest, Wheelchair
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.