# Roxwood Medical, Inc.

- Location (FDA's records): Redwood City, CA
- FDA decisions: 8 (2012–2017): 8 510(k) clearances
- Product codes: DQY (8)
- 510(k) review time since 2016: median 124 days, against 117 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 11 (6 its own); citations of its devices by later devices: 7 (6 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
- Radius Medical, LLC: 1 (https://510kreport.com/company/radius-medical)
- Vascular Solutions, Inc.: 1 (https://510kreport.com/company/vascular-solutions)
- Endocross, Ltd.: 1 (https://510kreport.com/company/endocross)
- Bridgepoint Medical: 1 (https://510kreport.com/company/bridgepoint-medical)
- Volcano Corporation: 1 (https://510kreport.com/company/volcano)

## Firms that cite its devices most
- Nitiloop, Ltd.: 1 (https://510kreport.com/company/nitiloop)

## Its most-cited devices
- K121763: Multicross Support Catheter (2012), cited by 3
- K140910: Centercross Catheter (2014), cited by 1
- K152456: CenterCross Ultra Catheter (2016), cited by 1
- K160681: CenterCross Ultra Catheter (2016), cited by 1
- K143744: MicroCross Catheter (2015), cited by 1

## Recent decisions
- K170403: CenterCross Ultra LV Catheter (Mar 7, 2017)
- K160681: CenterCross Ultra Catheter (Jun 17, 2016)
- K152957: MultiCross Catheter (Mar 4, 2016)
- K152456: CenterCross Ultra Catheter (Jan 26, 2016)
- K151082: MicroCross Catheter (Jun 7, 2015)
- K143744: MicroCross Catheter (Apr 14, 2015)
- K140910: Centercross Catheter (Nov 19, 2014)
- K121763: Multicross Support Catheter (Nov 27, 2012)

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