# Beijing Globalipl Development Co., Ltd.

- Location (FDA's records): Beijing, CN
- FDA decisions: 4 (2020–2022): 4 510(k) clearances
- Product codes: GEX (2), ONF (2)
- 510(k) review time since 2016: median 141 days, against 152 for FDA's reviews in the same codes and years (1 of 4 faster)
- Predicates its devices cite: 5 (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
- Beijing Adss Development Co., Ltd.: 2 (https://510kreport.com/company/beijing-adss-development)
- Shangdong Huamei Technology Co., Ltd.: 1 (https://510kreport.com/company/shangdong-huamei-technology)
- Shandong Huamei Technology Co., Ltd.: 1 (https://510kreport.com/company/shandong-huamei-technology)
- Beijing Superlaser Technology Co., Ltd.: 1 (https://510kreport.com/company/beijing-superlaser-technology)

## Recent decisions
- K222916: US 450  Diode Laser Equipment (Dec 9, 2022)
- K220385: Intense Pulsed Light Equipment (Aug 12, 2022)
- K212611: CO2 Laser Equipment (Feb 1, 2022)
- K193328: IPL + Diode Laser Machine (Mar 25, 2020)

Source page: https://510kreport.com/company/beijing-globalipl-development