4 devices · 1 company · 2023 to 2026
Manteia Technologies Co., Ltd.: AI-enabled devices on FDA's list
4 devices from Manteia Technologies Co., Ltd., 2023 to 2026, from 1 company across 2 product codes. 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.
Product codes from Manteia Technologies Co., Ltd.
Every device, newest decision first
| Decision | Device | Panel | Product code | FDA |
|---|---|---|---|---|
| AccuContour 4.0K251351 · 510(k) | Radiology | QKB | database entry | |
| ARTAssistantK250780 · 510(k) | Radiology | QKB | database entry | |
| MOZI TPSK223724 · 510(k) | Radiology | MUJ | database entry | |
| AccuContourK221706 · 510(k) | Radiology | QKB | database entry |
Every company in the record, the whole record of FDA AI-enabled medical devices, or what Apodicta does on a medical record.