# Dmc Medical, Ltd.

- Location (FDA's records): Fullerton, CA
- FDA decisions: 3 (2000–2011): 3 510(k) clearances
- Product codes: FMF (1), GBX (1), DWF (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 6 (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
- Icu Medical, Inc.: 1 (https://510kreport.com/company/icu-medical)
- Shiley, Inc.: 1 (https://510kreport.com/company/shiley)

## Firms that cite its devices most
- Procedure Products, Inc.: 1 (https://510kreport.com/company/procedure-products)
- Vescare, Inc.: 1 (https://510kreport.com/company/vescare)
- Maquet Cardiovascular, LLC: 1 (https://510kreport.com/company/maquet-cardiovascular)
- Mazza Healthcare, LLC: 1 (https://510kreport.com/company/mazza-healthcare)
- Shanghai Kindly Enterprise Development Group Co., Ltd.: 1 (https://510kreport.com/company/shanghai-kindly-enterprise-development-group)
- Moerae Matrix, Inc.: 1 (https://510kreport.com/company/moerae-matrix)

## Its most-cited devices
- K103736: DMC Medical Single-Use Polycarbonate Syringe (2011), cited by 3
- K000704: DMC Saphenous Vein Distention System (SVDS) (2000), cited by 3

## Recent decisions
- K103736: DMC Medical Single-Use Polycarbonate Syringe (Jun 10, 2011)
- K992932: Cipa (Adults) Cipi (Infants) (Jun 7, 2000)
- K000704: DMC Saphenous Vein Distention System (SVDS) (May 19, 2000)

Source page: https://510kreport.com/company/dmc-medical