# Lifetech Scientific (Shenzhen) Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 3 (2010–2013): 3 510(k) clearances
- Product codes: MMX (1), DRE (1), DQY (1)
- Predicates its devices cite: 5 (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
- Microvena Corp.: 1 (https://510kreport.com/company/microvena)
- Edwards Lifesciences, LLC: 1 (https://510kreport.com/company/edwards-lifesciences)
- Coombs Medical Device Consulting: 1 (https://510kreport.com/company/coombs-medical-device-consulting)
- Aga Medical Corp.: 1 (https://510kreport.com/company/aga-medical)
- Enpath Medical, Inc.: 1 (https://510kreport.com/company/enpath-medical)

## Firms that cite its devices most
- Cook, Inc.: 1 (https://510kreport.com/company/cook)

## Its most-cited devices
- K123842: Lawmax Dilator (2013), cited by 1

## Recent decisions
- K123842: Lawmax Dilator (Jun 24, 2013)
- K100184: Fustar Steerable Introducers (Feb 14, 2011)
- K102484: Sequre Snare System (Nov 9, 2010)

Source page: https://510kreport.com/company/lifetech-scientific-shenzhen