Data / Medical devices / United States / Golden Technologies, Inc
Golden Technologies, Inc: FDA-registered device maker in Old Forge, PA, United States, 1 510(k) clearance
Golden Technologies, Inc is registered with the FDA (registration 3006791235) 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. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006791235
- Address
- 525 Bridge Street, Old Forge, PA, United States, 18518
- Owner or operator
- GOLDEN BROTHERS, INC. (9925096)
- Roles
- Manufacturer, Manufacturer for export, Specification developer
- 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, Manufacturer for export, 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 14, 1988 | K880800 | GOLDEN POWER LIFT CHAIR | INO | Substantially Equivalent | Golden Technologies, Inc. | 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.