# Hebei Zhemai Technology Co., Ltd.

- Location (FDA's records): Langfang, CN
- FDA decisions: 3 (2023–2023): 3 510(k) clearances
- Product codes: GEX (2), ONF (1)
- 510(k) review time since 2016: median 86 days, against 87 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 2 (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
- Beijing Superlaser Technology Co., Ltd.: 1 (https://510kreport.com/company/beijing-superlaser-technology)
- Beijing HuaCheng Taike Technology Co., Ltd.: 1 (https://510kreport.com/company/beijing-huacheng-taike-technology)
- Beijing Adss Development Co., Ltd.: 1 (https://510kreport.com/company/beijing-adss-development)

## Firms that cite its devices most
- Hebei JT Medical Co., Ltd.: 1 (https://510kreport.com/company/hebei-jt-medical)
- Hebei Newangie Technology Co., Ltd.: 1 (https://510kreport.com/company/hebei-newangie-technology)

## Its most-cited devices
- K232709: Diode laser therapy device (2023), cited by 1
- K232716: Q-Switched Nd:Yag laser (2023), cited by 1

## Recent decisions
- K232708: Intense pulsed light therapy device (Dec 1, 2023)
- K232709: Diode laser therapy device (Nov 30, 2023)
- K232716: Q-Switched Nd:Yag laser (Nov 30, 2023)

Source page: https://510kreport.com/company/hebei-zhemai-technology