# Coaxia, Inc.

- Location (FDA's records): Maple Grove, MN
- FDA decisions: 2 (2003–2009): 2 510(k) clearances
- Product codes: MJN (2)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 3 (1 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
- Micro Therapeutics, Inc.: 1 (https://510kreport.com/company/micro-therapeutics)
- Heartport, Inc.: 1 (https://510kreport.com/company/heartport)
- Medical Components, Inc.: 1 (https://510kreport.com/company/medical-components)
- Radiant Medical: 1 (https://510kreport.com/company/radiant-medical)

## Firms that cite its devices most
- Thermopeutix, Inc.: 1 (https://510kreport.com/company/thermopeutix)
- Arch Catheter, LLC: 1 (https://510kreport.com/company/arch-catheter)

## Its most-cited devices
- K023914: Coaxia Flocontrol Catheter (2003), cited by 2
- K090970: Flocontrol , Model 1028 (2009), cited by 1

## Recent decisions
- K090970: Flocontrol , Model 1028 (Jun 12, 2009)
- K023914: Coaxia Flocontrol Catheter (Feb 21, 2003)

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