Data / Medical devices / Prosthesis, Thigh Socket, External Component / United States
FDA-registered makers of Prosthesis, Thigh Socket, External Component in the United States: 20 establishments
20 establishments in the United States are registered with the FDA to make Prosthesis, Thigh Socket, External Component (product code ISS). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Prosthesis, Thigh Socket, External Component
- Product code
- ISS
- Country
- United States
Makers of Prosthesis, Thigh Socket, External Component in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alps South LLC | Saint Petersburg, FL, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Anclote Manufacturing Company | Largo, FL, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Amparo Prosthetics, Inc. | West Valley City, UT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bracesox, The Original | Soquel, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| CJ Socket Technologies, Inc. | Beverly, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Invent Medical Usa, LLC | Warminster, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| L&R Usa Inc. | Milwaukee, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Martin Bionics Innovations, LLC | Oklahoma City, OK, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orthomerica Products, Inc. | Orlando, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Otto Bock Healthcare LP | Salt Lake City, UT, United States | Contract manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ossur Orlando | Orlando, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Proteor Usa | Tempe, AZ, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PROTEOR USA, Gunnison | Gunnison, UT, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Protosthetics | Fargo, ND, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Slingshot Bionics | Oklahoma City, OK, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Spinal Systems, LLC | Louisville, KY, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Symbiont Logistics, LLC | Phoenix, AZ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tiburon Medical Enterprises | San Jacinto, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Thuasne, LLC | Kansas City, KS, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| WillowWood Global LLC | Mt Sterling, OH, 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.