Data / Medical devices / United States / Golden Brothers, Inc
Golden Brothers, Inc: FDA-registered device maker in Old Forge, PA, United States, 1 510(k) clearance
Golden Brothers, Inc is registered with the FDA (registration 2523955) in Old Forge, PA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 14, 1988. 2 recall events name it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2523955
- Address
- 401 Bridge St, Old Forge, PA, United States, 18518
- Owner or operator
- GOLDEN BROTHERS, INC. (9925096)
- Roles
- Manufacturer
- First device listed
- August 31, 2005
- Registered through
- 2026
- Brand names listed
- GOLDEN POWER LIFT CHAIR
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chair, Positioning, Electric | INO | 2 | Manufacturer | 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 14, 1988 | K880800 | GOLDEN POWER LIFT CHAIR | INO | Substantially Equivalent | Golden Technologies, 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 |
|---|---|---|---|---|---|---|
| July 6, 2020 | 86106 | Class II | Terminated | Golden Technologies Model Number PR515 Lift Chair - Product Usage: is to provide lift assistance for persons who have difficulty rising from a seated position to a standing position. | Suspect poor weld on back KD bar. | accessdata.fda.gov |
| January 21, 2014 | 67416 | Class II | Terminated | Buzzaround XL scooters' Product Usage: mobility | Buzzaround XL scooters' front to rear lockup can become unintentionally disengaged due to possible improper fit of the front alignment cup to the rear alignment screw. | accessdata.fda.gov |
Compare with other makers
Updated March 14, 1988. 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.