# See-Mode Technologies Pte, Ltd.

- Location (FDA's records): Singapore, SG
- FDA decisions: 3 (2020–2026): 3 510(k) clearances
- Names in FDA's records: See-Mode Technologies Pte, Ltd. (2); See-Mode Technologies Pty, Ltd. (1)
- Product codes: QDQ (2), LLZ (1)
- 510(k) review time since 2016: median 179 days, against 153 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (0 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
- Taihao Medical, Inc.: 2 (https://510kreport.com/company/taihao-medical)
- Atheropoint, LLC: 1 (https://510kreport.com/company/atheropoint)

## Recent decisions
- K260303: See-Mode Augmented Reporting Tool, Breast (SMART-B) (Jul 28, 2026)
- K240697: See-Mode Augmented Reporting Tool, Thyroid (SMART-T) (Sep 9, 2024)
- K201369: AVA (Augmented Vascular Analysis) (Sep 16, 2020)

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