Data / Medical devices / United States / Golden Brothers, Inc.
Golden Brothers, Inc.: FDA-registered device maker in Plains Township, PA, United States, 7 510(k) clearances
Golden Brothers, Inc. is registered with the FDA (registration 3008812160) in Plains Township, PA, United States. It lists 2 device types. The FDA files 7 510(k) clearances under its listings, the newest dated March 22, 2007. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3008812160
- Address
- 1112 Inkerman Road, Plains Township, PA, United States, 18702
- Owner or operator
- GOLDEN BROTHERS, INC. (9925096)
- Roles
- Manufacturer, Specification developer
- First device listed
- May 1, 2000
- Registered through
- 2026
- Brand names listed
- Alante Sport GP208, Alante Sport GP209, Avenger, Buzz About GP164, Buzzaround Carryon Foldable GP130, Buzzaround GB107, Buzzaround GB117, Buzzaround GB118 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Vehicle, Motorized 3-Wheeled | INI | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Wheelchair, Powered | ITI | 2 | Specification developer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 22, 2007 | K070501 | RUIKE 3421 POWERED WHEELCHAIR | ITI | Substantially Equivalent | Shanghai Ruike Sports Goods Co., Ltd. | accessdata.fda.gov |
| November 2, 2006 | K063162 | GOLDEN LITEWAY | INI | Substantially Equivalent | Golden Technologies, Inc. | accessdata.fda.gov |
| June 3, 2004 | K041341 | GOLDEN SPYDER, MODEL GS-300 | ITI | Substantially Equivalent | Golden Technologies, Inc. | accessdata.fda.gov |
| May 3, 2004 | K041025 | BUZZAROUND, VEHICLE, MOTORIZED 3-WHEELED | INI | Substantially Equivalent | Golden Technologies, Inc. | accessdata.fda.gov |
| December 3, 2001 | K012258 | COMPANION MODEL 221, 321, 421 | INI | Substantially Equivalent | Golden Technologies, Inc. | accessdata.fda.gov |
| May 29, 2001 | K011153 | ALANTE, BATTERY OPERATED POWER WHEELCHAIR | ITI | Substantially Equivalent | Golden Technologies, Inc. | accessdata.fda.gov |
| July 23, 1997 | K971387 | FREERIDER, MODEL FR510-F | INI | Substantially Equivalent | Freerider USA, Inc. | accessdata.fda.gov |
Compare with other makers
Updated March 22, 2007. 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.