Data / Medical devices / Wheelchair, Standup / United States
FDA-registered makers of Wheelchair, Standup in the United States: 6 establishments
6 establishments in the United States are registered with the FDA to make Wheelchair, Standup (product code IPL). 6 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Wheelchair, Standup
- Product code
- IPL
- Country
- United States
Makers of Wheelchair, Standup in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| ATZ Manufacturing | Marshall, MN, United States | Manufacturer | 2 | February 10, 2022 | 0 | 0 | 0 | api.fda.gov |
| Matia Robotics (us), Inc. | Salt Lake City, UT, United States | Manufacturer | 2 | May 29, 2020 | 0 | 0 | 0 | api.fda.gov |
| Permobil, Inc. | Lebanon, TN, United States | Manufacturer | 2 | February 27, 2020 | 0 | 0 | 0 | api.fda.gov |
| The Standing Company | Saginaw, MI, United States | Manufacturer | 2 | January 22, 2004 | 0 | 1 | 0 | api.fda.gov |
| Sunrise Medical (us) LLC | Fresno, CA, United States | Complaint file establishment, Specification developer | 1 | January 16, 2018 | 0 | 0 | 0 | api.fda.gov |
| Sunrise Medical (US) LLC | Mount Juliet, TN, United States | Complaint file establishment, Manufacturer | 1 | January 16, 2018 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.