Data / Medical devices / Image Acquisition And/Or Optimization Guided By Artificial Intelligence
Image Acquisition And/Or Optimization Guided By Artificial Intelligence (QJU): 4 FDA-registered makers in 4 countries
4 establishments in 4 countries are registered with the FDA to make Image Acquisition And/Or Optimization Guided By Artificial Intelligence (product code QJU, Class 2, 21 CFR 892.2100). 4 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 10 510(k) clearances under this code, the latest on October 2, 2026, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- QJU
- Device class
- 2
- Regulation
- 892.2100
- Medical specialty
- Radiology
Makers by country
| Country | Makers |
|---|---|
| United States | 1 |
| France | 1 |
| Israel | 1 |
| Germany | 1 |
Makers of Image Acquisition And/Or Optimization Guided By Artificial Intelligence
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 |
|---|---|---|---|---|---|---|---|---|
| GE Medical Systems Ultrasound and Primary Care Diagnostics, LLC | Waukesha, WI, United States | Manufacturer | 3 | October 2, 2026 | 0 | 0 | 0 | api.fda.gov |
| DESKi SAS | Bordeaux Nouvelle-Aquitaine, France | Complaint file establishment, Manufacturer | 2 | June 3, 2026 | 0 | 0 | 0 | api.fda.gov |
| Ultrasight | Ness Ziona Central, Israel | Manufacturer | 2 | December 17, 2025 | 0 | 0 | 0 | api.fda.gov |
| Thinksono GMBH | Potsdam Brandenburg, Germany | Manufacturer | 1 | July 15, 2026 | 0 | 0 | 0 | api.fda.gov |
Updated October 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.