Data / Medical devices / Prosthesis, Hip, Femoral, Resurfacing / United States
FDA-registered makers of Prosthesis, Hip, Femoral, Resurfacing in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Prosthesis, Hip, Femoral, Resurfacing (product code KXA). 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
- Prosthesis, Hip, Femoral, Resurfacing
- Product code
- KXA
- Country
- United States
Makers of Prosthesis, Hip, Femoral, Resurfacing in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Microport Orthopedics Inc. | Arlington, TN, United States | Manufacturer | 3 | December 12, 2008 | 0 | 0 | 0 | api.fda.gov |
| Arthrosurface, Inc. | W Bridgewater, MA, United States | Manufacturer | 1 | August 1, 2002 | 0 | 0 | 0 | api.fda.gov |
| Biocore9 LLC | Denville, NJ, United States | Manufacturer | 1 | January 19, 2021 | 0 | 0 | 0 | api.fda.gov |
| Biopro, Inc. | Port Huron, MI, United States | Contract manufacturer, Manufacturer | 1 | May 18, 2005 | 0 | 0 | 0 | api.fda.gov |
| E. Bac Si Imports LLC | Ellensburg, WA, United States | Specification developer | 1 | May 23, 1991 | 0 | 0 | 0 | api.fda.gov |
| Zimmer, Inc. | Warsaw, IN, United States | Manufacturer | 1 | April 13, 1995 | 0 | 2 | 0 | api.fda.gov |
| Aps Materials, Inc. | Dayton, OH, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Donson Machine Company | Alsip, IL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Primo Medical Group, INC | Stoughton, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Symmetry Medical Manufacturing Inc | Claypool, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Symmetry Medical Manufacturing Inc. | Warsaw, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Viant AS&O Holdings, LLC | Brimfield, MA, United States | Contract 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.