# Shenzhen Yolanda Technology Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 3 (2022–2023): 3 510(k) clearances
- Product codes: DXN (2), FLL (1)
- 510(k) review time since 2016: median 153 days, against 182 for FDA's reviews in the same codes and years (3 of 3 faster)
- Predicates its devices cite: 0 (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

## Recent decisions
- K230176: Upper Arm Blood Pressure Monitor (Jun 29, 2023)
- K221211: Infrared thermometer (Sep 27, 2022)
- K221212: Upper Arm Blood Pressure Monitor (Aug 26, 2022)

Source page: https://510kreport.com/company/shenzhen-yolanda-technology