Data / Medical devices / Israel / Upnride Robotics Ltd
Upnride Robotics Ltd: FDA-registered device maker in Yokneam Illit Northern, Israel, 1 510(k) clearance
Upnride Robotics Ltd is registered with the FDA (registration 3014890685) in Yokneam Illit Northern, Israel. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 12, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014890685
- Address
- Kochav Yokneam Building, Yokneam Illit Northern, Israel, 20692 04
- Owner or operator
- UPnRIDE Robotics Ltd (10094206)
- Roles
- Manufacturer
- First device listed
- November 19, 2025
- Registered through
- 2026
- Brand names listed
- UPnRIDE, UPnRIDE 1.1 stand-up power wheelchair, UPnRIDE power wheelchair, UPnRIDE stand-up power wheelchair
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Standup | IPL | 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 |
|---|---|---|---|---|---|---|
| September 12, 2019 | K182257 | UPnRIDE | IPL | Substantially Equivalent | Upnride Robotics , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated September 12, 2019. 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.