# Endocross, Ltd.

- Location (FDA's records): Washington, DC
- FDA decisions: 3 (2008–2009): 3 510(k) clearances
- Product codes: DQY (3)
- Predicates its devices cite: 9 (3 its own); citations of its devices by later devices: 6 (3 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
- Asahi Intecc Co., Ltd.: 2 (https://510kreport.com/company/asahi-intecc)
- Medtronics Interventional Vascular: 1 (https://510kreport.com/company/medtronics-interventional-vascular)
- Angiometrx, Inc.: 1 (https://510kreport.com/company/angiometrx)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Intra Luminal Therapeutics, Inc.: 1 (https://510kreport.com/company/intra-luminal-therapeutics)

## Firms that cite its devices most
- Upstream Peripheral Technologies: 1 (https://510kreport.com/company/upstream-peripheral-technologies)
- Roxwood Medical, Inc.: 1 (https://510kreport.com/company/roxwood-medical)
- Cruzar Medsystems, Inc.: 1 (https://510kreport.com/company/cruzar-medsystems)

## Its most-cited devices
- K082339: Enabler-P Support Catheter (2008), cited by 3
- K083833: Enabler-P Catheter, 1000 Part Number:1160 (2009), cited by 2
- K092174: Enabler-P Catheter System, Model 3000 (2009), cited by 1

## Recent decisions
- K092174: Enabler-P Catheter System, Model 3000 (Dec 30, 2009)
- K083833: Enabler-P Catheter, 1000 Part Number:1160 (May 22, 2009)
- K082339: Enabler-P Support Catheter (Nov 20, 2008)

Source page: https://510kreport.com/company/endocross