Data / Medical devices / China / Quality Life Technologies Co., Ltd.
Quality Life Technologies Co., Ltd.: FDA-registered device maker in Dongguan Guangdong, China, 4 510(k) clearances
Quality Life Technologies Co., Ltd. is registered with the FDA (registration 3008717361) in Dongguan Guangdong, China. It lists 10 device types. The FDA files 4 510(k) clearances under its listings, the newest dated November 2, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008717361
- Address
- Building 1, No.8, Quling Middle Road Liaobu Town, Dongguan City, Dongguan Guangdong, China, 523425
- Owner or operator
- QUALITY LIFE TECHNOLOGIES CO., LTD. (10037536)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- November 2, 2011
- Registered through
- 2026
- Brand names listed
- Electric Scooter, Holder, Powered Scooter, Powered Wheelchair, Wheelchair Accessories, Wheelchair Anti-Tip, Wheelchair Armrest, Wheelchair Belt and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Wheelchair | KNO | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Armrest, Wheelchair | IML | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Belt, Wheelchair | IQB | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Climber, Curb, Wheelchair | IMN | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Components, Wheelchair | KNN | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Device, Anti-Tip, Wheelchair | IMR | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Footrest, Wheelchair | IMM | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Holder, Crutch And Cane, Wheelchair | IMZ | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Vehicle, Motorized 3-Wheeled | INI | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Wheelchair, Powered | ITI | 2 | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| 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 |
| 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 |
Compare with other makers
- All makers of Footrest, Wheelchair
- All makers of Holder, Crutch And Cane, Wheelchair
- All makers of Wheelchair, Powered
- All makers of Belt, Wheelchair
- All makers of Accessories, Wheelchair
- All makers of Vehicle, Motorized 3-Wheeled
Updated November 2, 2006. 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.