Data / Medical devices / Chair, Positioning, Electric / United States
FDA-registered makers of Chair, Positioning, Electric in the United States: 13 establishments
13 establishments in the United States are registered with the FDA to make Chair, Positioning, Electric (product code INO). 10 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.
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- Device
- Chair, Positioning, Electric
- Product code
- INO
- Country
- United States
Makers of Chair, Positioning, Electric in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Pride Mobility Products Corp. | North Las Vegas, NV, United States | Manufacturer | 4 | December 2, 2009 | 0 | 0 | 0 | api.fda.gov |
| Pride Mobility Products Corp. | Duryea, PA, United States | Manufacturer, Specification developer | 4 | December 2, 2009 | 0 | 0 | 0 | api.fda.gov |
| Pride Mobility Products Corporation | North Las Vegas, NV, United States | Manufacturer | 4 | December 2, 2009 | 0 | 0 | 0 | api.fda.gov |
| Altimate Medical, Inc. | Morton, MN, United States | Manufacturer | 3 | August 13, 2013 | 0 | 1 | 0 | api.fda.gov |
| Mega Motion, Inc. | Duryea, PA, United States | Manufacturer | 2 | December 2, 2009 | 0 | 0 | 0 | api.fda.gov |
| Pride Mobility Products Corporation | Pontotoc, MS, United States | Manufacturer | 2 | December 2, 2009 | 0 | 0 | 0 | api.fda.gov |
| Design Specific Us Inc | Wilmington, DE, United States | Specification developer | 1 | December 23, 2010 | 0 | 0 | 0 | api.fda.gov |
| Golden Brothers, Inc | Old Forge, PA, United States | Manufacturer | 1 | March 14, 1988 | 0 | 1 | 0 | api.fda.gov |
| Golden Technologies, Inc | Old Forge, PA, United States | Manufacturer, Manufacturer for export, Specification developer | 1 | March 14, 1988 | 0 | 0 | 0 | api.fda.gov |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 1 | September 22, 2000 | 0 | 0 | 0 | api.fda.gov |
| Optima Products, Inc. | Saint Louis Park, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Medical | Portage, MI, United States | Complaint file establishment, Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| TPM Research | Homewood, AL, United States | Manufacturer | 0 | 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.