Data / Medical devices / Taiwan / Freerider, Corp.
Freerider, Corp.: FDA-registered device maker in Kaohsiung, Taiwan, 5 510(k) clearances
Freerider, Corp. is registered with the FDA (registration 3003820676) in Kaohsiung, Taiwan. It lists 7 device types. The FDA files 5 510(k) clearances under its listings, the newest dated March 20, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003820676
- Address
- No. 22 Bengong 5th Road GAN-SHAN Dist, Kaohsiung, Taiwan, 820
- Owner or operator
- FREERIDER, CORP. (9030042)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- October 29, 1999
- Registered through
- 2026
- Brand names listed
- Crutch holder, FR1 (Models FR1-13; FR1-15; FR1-17), FR510-F, Luggie, Luggie Chair, Luggie Super, Seat Belt, battery bag, Home docking station, foldable bag, memory seat cushion and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Wheelchair | KNO | 1 | Manufacturer | accessdata.fda.gov |
| Armrest, Wheelchair | IML | 1 | Manufacturer | accessdata.fda.gov |
| Belt, Wheelchair | IQB | 1 | Repackager or relabeler | accessdata.fda.gov |
| Components, Wheelchair | KNN | 1 | Manufacturer | accessdata.fda.gov |
| Holder, Crutch And Cane, Wheelchair | IMZ | 1 | Manufacturer | accessdata.fda.gov |
| Vehicle, Motorized 3-Wheeled | INI | 2 | Manufacturer | accessdata.fda.gov |
| Wheelchair, Powered | ITI | 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 20, 2017 | K160139 | Luggie Chair | ITI | Substantially Equivalent | Freerider Corporation | accessdata.fda.gov |
| September 10, 2015 | K151944 | Luggie Super | INI | Substantially Equivalent | Freerider Corporation | accessdata.fda.gov |
| January 8, 2015 | K133187 | FREERIDER FR1, models FR1-13, FR1-15, FR1-17 | INI | Substantially Equivalent | Freerider Corp | accessdata.fda.gov |
| September 30, 2011 | K110165 | FREERIDER MODEL LUGGIE MODEL 168-4IT | INI | Substantially Equivalent | Freerider Luggie Scooters, 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
- All makers of Vehicle, Motorized 3-Wheeled
- All makers of Armrest, Wheelchair
- All makers of Accessories, Wheelchair
- All makers of Components, Wheelchair
- All makers of Belt, Wheelchair
- All makers of Holder, Crutch And Cane, Wheelchair
Updated March 20, 2017. 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.