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PRIDE MOBILITY PRODUCTS CORP.

United States·US-MF-000008467

Last updated September 17, 2026

What PRIDE MOBILITY PRODUCTS CORP. makes

The company manufactures electric stand-up chairs, electric-motor-driven mobility scooters, occupant-controlled electric wheelchairs, and non-bariatric push-rim manual wheelchairs. It also produces assistive devices for input-control training, wheelchair steering/control units, noninvasive battery chargers, and timer switches for medical use.

These products are classified as Class I and Class II devices under regulatory frameworks. They are listed in the EU’s eudamed registry, the FDA’s 510(k) clearance database, and the FDA’s Unique Device Identifier (UDI) system. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country: United States
Address: 401 York Avenue, Duryea, United States
Website: www.pridemobility.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 001 800 800 8586
PRRC Contact: Kelly Livingston
EUDAMED SRN: US-MF-000008467
FDA FEI Number: 3007608806
DUNS Number: —

Catalogue (319)

Page 3 of 7

Device	Model / Reference	Registries	Class	Status
L225	L225	FDA UDI	Class II	Active
Mm6410	MM6410	FDA UDI	Class II	Active
Mm101	MM101	FDA UDI	Class II	Unknown
Lc158	LC158	FDA UDI	Class II	Active
Go Go Sport 3 Wheel	S73/Go Go ET Sport/Beaufort 6	FDA UDI	Class II	Active
Quantum 6000Z	Q6000Z/Q6000ZRQ/Q600 Sport	FDA UDI	Class II	Active
Twister	TWISTER	FDA UDI	Class I	Active
Mm3975	MM3975	FDA UDI	Class II	Active
Mm7001	MM7001	FDA UDI	Class II	Active
PLR990iL	PLR990iL	FDA UDI	Class II	Active
Plr935pw	PLR935PW	FDA UDI	Class II	Active
Lc670	LC670	FDA UDI	Class II	Active
Lc358pw	LC358PW/CA358PW	FDA UDI	Class II	Active
Celebrity DX 3 Wheel	SC4001DX/S4001DX	FDA UDI	Class II	Active
C6	C6	FDA UDI	Class II	Active
Lc358s	LC358S/CA358S	FDA UDI	Class II	Active
Mm4001	MM4001	FDA UDI	Class II	Active
Cl500	CL500	FDA UDI	Class II	Active
Elegance	PLR975	FDA UDI	Class II	Unknown
Lc450	LC450	FDA UDI	Class II	Active
Elite Traveller 2 Platinum	SC442EMS	FDA UDI	Class II	Active
Maxima 3 Wheel	SC900/S900	FDA UDI	Class II	Active
Sr525l	SR525L	FDA UDI	Class II	Active
FrontRunner	FrontRunner	FDA UDI	Class II	Active
Lc570w	LC570W	FDA UDI	Class II	Active
Q6 Edge 320 Stretto	Q6 Edge 320 Stretto	FDA UDI	Class II	Unknown
Mm6405	MM6405	FDA UDI	Class II	Active
UK660i	UK660i	FDA UDI	Class II	Active
Lc435l	LC435L	FDA UDI	Class II	Active
Sr525m	SR525M	FDA UDI	Class II	Active
UKD30i	UKD30i	FDA UDI	Class II	Active
Rascal Carbon Cruiser	Rascal Carbon Cruiser	FDA UDI	Class II	Active
Lc580l	LC580L	FDA UDI	Class II	Active
Jazzy 1450	Jazzy 1450	FDA UDI	Class II	Active
Urbana	PLR965	FDA UDI	Class II	Unknown
Usb Charger	USB CHARGER	FDA UDI	Class I	Active
GoGo Carbon (SC25M)	GoGo Carbon (SC25M)	FDA UDI	Class II	Active
Lc465m	LC465M	FDA UDI	Class II	Active
Rascal Conquest	RSC103	FDA UDI	Class II	Active
Mm3702	MM3702	FDA UDI	Class II	Active
Mm2750	MM2750	FDA UDI	Class II	Active
Lc485	LC485	FDA UDI	Class II	Active
S2525l	S2525L	FDA UDI	Class II	Active
Mm3615	MM3615	FDA UDI	Class II	Active
Plr4955m	PLR4955M	FDA UDI	Class II	Active
Mm6100so	MM6100SO	FDA UDI	Class II	Active
Jazzy Air	Jazzy Air	FDA UDI	Class II	Active
J6	J6	FDA UDI	Class II	Active
Mm3710	MM3710	FDA UDI	Class II	Active
LC575iM	LC575iM	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

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Authorities

Not available yet.

FDA Recalls (8)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Pride Mobility Products Corp. has eight recall records listed in the FDA database, all initiated between June 7, 2004, and December 1, 2016, with each record marked as terminated. The reasons cited include mechanical failures such as separation of the tilt base interface, missing or improper harness components allowing water ingress, misaligned wire harnesses risking pinching or short circuits, potential overheating from torn heating pads, disabled software safety features, and noncompliance with component specifications due to a contract manufacturer error.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Dec 1, 2016	Z-0942-2017	—	terminated	The interface between the TB3 back and tilt base can separate when tilted beyond the specified angle.
Jun 22, 2011	Z-3211-2011	—	terminated	Contract manufacturer error. Component part(s) (fuses) specifications were not adhered to as outlined in Pride's Engineering drawings.
Jun 22, 2011	Z-3212-2011	—	terminated	Contract manufacturer error. Component part(s) (fuses) specifications were not adhered to as outlined in Pride's Engineering drawings.
Nov 26, 2010	Z-1941-2012	—	terminated	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.
Feb 1, 2010	Z-2619-2010	—	terminated	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.
Feb 1, 2010	Z-2618-2010	—	terminated	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.
Apr 11, 2008	Z-1776-2008	—	terminated	Software - Watch dog timer feature was disabled.
Jun 7, 2004	Z-0212-05	—	terminated	The heating pad on these Lift Chairs may tear at the entry point causing a short and/or overheating, which can damage the chair.