# Beijing Demax Medical Technology Co.,Ltd

- Location (FDA's records): Beijing, CN
- FDA decisions: 4 (2015–2024): 4 510(k) clearances
- Product codes: DYB (2), MAV (1), DXC (1)
- 510(k) review time since 2016: median 166 days, against 56 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: 1 (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
- Merit Medical Systems, Inc.: 2 (https://510kreport.com/company/merit-medical-systems)
- Atrion Medical Products, Inc.: 1 (https://510kreport.com/company/atrion-medical-products)

## Firms that cite its devices most
- Ningbo Dizegens Medical Science Co.,Ltd: 1 (https://510kreport.com/company/ningbo-dizegens-medical-science)

## Its most-cited devices
- K222182: Radial Artery Compression Tourniquets (2023), cited by 1

## Recent decisions
- K242248: Introducer Sheath Kits (Aug 22, 2024)
- K222184: Introducer Sheath Kits (Feb 21, 2023)
- K222182: Radial Artery Compression Tourniquets (Jan 4, 2023)
- K140943: Mastro Plus Balloon in-Deflation Device (Mar 5, 2015)

Source page: https://510kreport.com/company/beijing-demax-medical-technology