# Shenzhen Lifotronic Technology Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 3 (2020–2026): 3 510(k) clearances
- Product codes: IRP (1), GEX (1), PDJ (1)
- Predicates its devices cite: 4 (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
- Daesung Maref Co., Ltd.: 1 (https://510kreport.com/company/daesung-maref)
- Shenzhen Aozemei Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-aozemei-technology)
- Li-Tek Electronics Technologies: 1 (https://510kreport.com/company/li-tek-electronics-technologies)
- Shenzhen Nuon Medical Equipment Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-nuon-medical-equipment)

## Recent decisions
- K260468: H100Plus Hemoglobin Testing System (Oct 2, 2026)
- K251076: Diode Laser Hair Removal Machine (models: T60A, T60B, T60C, T60D, T60E) (Jul 30, 2025)
- K192466: Air Compression Therapy System (Jun 22, 2020)

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