Data / Medical devices / Radiological Image Processing Software For Ablation Therapy Planning And Evaluation
Radiological Image Processing Software For Ablation Therapy Planning And Evaluation (QTZ): 6 FDA-registered makers in 3 countries
6 establishments in 3 countries are registered with the FDA to make Radiological Image Processing Software For Ablation Therapy Planning And Evaluation (product code QTZ, Class 2, 21 CFR 892.2050). 4 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 9 510(k) clearances under this code, the latest on June 16, 2026, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- QTZ
- Device class
- 2
- Regulation
- 892.2050
- Medical specialty
- Radiology
Makers by country
| Country | Makers |
|---|---|
| United States | 4 |
| Germany | 1 |
| Israel | 1 |
Makers of Radiological Image Processing Software For Ablation Therapy Planning And Evaluation
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Siemens Healthineers AG Varian Cancer Therapy (CTH) | Erlangen Bavaria, Germany | Manufacturer | 2 | June 16, 2026 | 0 | 0 | 0 | api.fda.gov |
| Eigen | Grass Valley, CA, United States | Manufacturer | 1 | October 12, 2023 | 0 | 0 | 0 | api.fda.gov |
| Mim Software Inc. | Cleveland, OH, United States | Complaint file establishment, Manufacturer | 1 | October 7, 2022 | 0 | 0 | 0 | api.fda.gov |
| Techsomed | Or Yehuda Central, Israel | Manufacturer | 1 | September 8, 2025 | 0 | 0 | 0 | api.fda.gov |
| Avnet, Inc. (Avnet Logistics) | Chandler, AZ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips DS North America LLC | Gainesville, FL, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated June 16, 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.