4 devices · 2 companies · 2023 to 2026
Magentiq Eye, Ltd.: AI-enabled devices on FDA's list
4 devices from Magentiq Eye, Ltd., 2023 to 2026, from 2 companies across 1 product code. Each record carries FDA's decision, the Indications for Use statement verbatim where the public document carries one (4 of 4 here), the regulation, and MAUDE report counts by product code.
Retrieved from FDA public records.
Every device, newest decision first
| Decision | Device | Panel | Product code | FDA |
|---|---|---|---|---|
| MAGENTIQ-COLOK260724 · 510(k) | Gastroenterology-Urology | QNP | database entry | |
| MAGENTIQ-COLOK252178 · 510(k) | Gastroenterology-Urology | QNP | database entry | |
| MAGENTIQ-COLOK244023 · 510(k) | Gastroenterology-Urology | QNP | database entry | |
| ME-APDSK223473 · 510(k) | Gastroenterology-Urology | QNP | database entry |
Every company in the record, the whole record of FDA AI-enabled medical devices, or what Apodicta does on a medical record.