# Shenzhen Witleaf Medical Electronics Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 2 (2022–2023): 2 510(k) clearances
- Product codes: DQA (2)
- Predicates its devices cite: 2 (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
- Shenzhen Hexin Zondan Medical Equipment Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-hexin-zondan-medical-equipment)
- Shenzhen Creative Industry Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-creative-industry)

## Recent decisions
- K213431: Handheld Pulse Oximeter (Feb 26, 2023)
- K213430: Fingertip Pulse Oximeter (Dec 30, 2022)

Source page: https://510kreport.com/company/shenzhen-witleaf-medical-electronics