Data / Medical devices / Block, Beam-Shaping, Radiation Therapy / United States
FDA-registered makers of Block, Beam-Shaping, Radiation Therapy in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Block, Beam-Shaping, Radiation Therapy (product code IXI). 8 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
- Block, Beam-Shaping, Radiation Therapy
- Product code
- IXI
- Country
- United States
Makers of Block, Beam-Shaping, Radiation Therapy in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| CQ Decimal, LLC | Sanford, FL, United States | Manufacturer | 7 | October 16, 2013 | 0 | 0 | 0 | api.fda.gov |
| Aktina Medical Corp. | Congers, NY, United States | Manufacturer | 2 | February 10, 1998 | 0 | 0 | 0 | api.fda.gov |
| Huestis Machine Corp. | Bristol, RI, United States | Manufacturer | 2 | May 31, 1990 | 0 | 0 | 0 | api.fda.gov |
| Medical Modeling - A 3D Systems Company | Littleton, CO, United States | Manufacturer | 1 | March 30, 2022 | 0 | 0 | 0 | api.fda.gov |
| Myrava, LLC | Indianapolis, IN, United States | Manufacturer | 1 | April 6, 2026 | 0 | 0 | 0 | api.fda.gov |
| Myrava, LLC | Winston Salem, NC, United States | Manufacturer | 1 | April 6, 2026 | 0 | 0 | 0 | api.fda.gov |
| Myrava, LLC | Parma, OH, United States | Manufacturer | 1 | April 6, 2026 | 0 | 0 | 0 | api.fda.gov |
| VHA Office of Advanced Manufacturing - Ft. Lawton | Seattle, WA, United States | Manufacturer | 1 | November 4, 2022 | 0 | 0 | 0 | api.fda.gov |
| Elekta Inc. | San Jose, CA, 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.