Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008812160

FEI Number

3008812160

Entity Name

GOLDEN BROTHERS, INC.

City/State/Country

Plains Township, PA, US

Establishment Address

1112 Inkerman Road, Plains Township, PA 18702, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

GOLDEN BROTHERS, INC. (Owner Number: 9925096)

Owner / Operator Contact Address

401 BRIDGE ST., --, Old Forge, PA 18518, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K041025

PMA Number

N/A

All Registered Proprietary Names

Alante Sport GP209 Alante Sport GP208 Literider Envy GP162 Buzz About GP164 Envy Lite GP161 COMPASS GP620 Compass Sport GP605 Buzzaround GB118 Buzzaround GB117 Buzzaround GB119 Buzzaround GB148 Buzzaround LT GB124 Buzzaround GB147 Buzzaround GB149 Buzzaround GB107 Buzzaround LT GB121 Buzzaround GB120 Buzzaround GB220

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ITI	Wheelchair, Powered	Physical Medicine	Class 2	890.3860	2010-03-19
ITI	Wheelchair, Powered	Physical Medicine	Class 2	890.3860	2000-05-01
INI	Vehicle, Motorized 3-Wheeled	Physical Medicine	Class 2	890.3800	2005-08-31

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GOLDEN BROTHERS, INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3006791235	Golden Technologies, Inc	Old Forge, PA, US
2523955	Golden Brothers, Inc	OLD FORGE, PA, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K853594	Vessa , Ltd.	VESSA FLIVVA	1985-09-24
K142783	Heartway Medical Products Co., Ltd.	HEARTWAY Electrically Powered Wheelchair P27	2015-06-12

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0005-2018	Permobil, Ab Arvaltsvagen 10	2	Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR
Z-0006-2018	Permobil, Ab Arvaltsvagen 10	2	Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500
Z-0039-2007	Eagle Parts and Products	2	Eagle Parts and Products Model 624EZ Power Wheel Chairs with internally threaded wheel mount motors.
Z-0040-2007	Eagle Parts and Products	2	Eagle Parts and Products Model 624Mini Power Wheel Chairs with internally threaded wheel mount motors.
Z-0036-2007	Medline Industries Inc	2	Medline Strider Maxi 3 Scooter; a three wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung, Taiwan for Medline Industries, Inc., One Medline Place, Mundelein, IL 60060 USA; model MDS807600 - red and MDS807600B - blue

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008812160. Last updated year: 2026. Please use registration number 3008812160 when referencing this establishment in official correspondence.