Data / Medical devices / Hand, External Limb Component, Powered / United States
FDA-registered makers of Hand, External Limb Component, Powered in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Hand, External Limb Component, Powered (product code IQZ). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Hand, External Limb Component, Powered
- Product code
- IQZ
- Country
- United States
Makers of Hand, External Limb Component, Powered in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alt-Bionics, Inc. | San Antonio, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Covvi Usa, Inc | San Antonio, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Coapt LLC | Chicago, IL, United States | Complaint file establishment, Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hugh Steeper Ltd DBA SteeperUSA | Hopkinton, MA, United States | Complaint file establishment, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Infinite Biomedical Technologies, LLC | Baltimore, MD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Motion Control, Inc. | Salt Lake City, UT, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Myomo, Inc. | Burlington, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ossur Americas | West Deptford, NJ, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Psyonic | San Diego, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.