# Manteia Technologies Co., Ltd.

- Location (FDA's records): Xiamen, CN
- FDA decisions: 7 (2023–2026): 7 510(k) clearances
- Product codes: QKB (3), IYE (3), MUJ (1)
- 510(k) review time since 2016: median 231 days, against 140 for FDA's reviews in the same codes and years (0 of 7 faster)
- Predicates its devices cite: 7 (3 its own); citations of its devices by later devices: 3 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Varian Medical Systems, Inc.: 3 (https://510kreport.com/company/varian-medical-systems)
- Xiamen Manteia Technology, Ltd.: 1 (https://510kreport.com/company/xiamen-manteia-technology)

## Its most-cited devices
- K221706: AccuContour (2023), cited by 2
- K223834: AccuCheck (2023), cited by 1

## Recent decisions
- K260733: MRIA Radiation Therapy Information System (MRIA) (Aug 26, 2026)
- K251351: AccuContour 4.0 (Jan 23, 2026)
- K250780: ARTAssistant (Dec 5, 2025)
- K250696: AccuCheck (Oct 24, 2025)
- K223834: AccuCheck (Jul 20, 2023)
- K223724: Mozi TPS (Jul 10, 2023)
- K221706: AccuContour (Mar 9, 2023)

Source page: https://510kreport.com/company/manteia-technologies