# Veinrx, Inc.

- Location (FDA's records): Miami, FL
- FDA decisions: 2 (2005–2007): 2 510(k) clearances
- Product codes: KRA (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (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
- Id, LLC: 2 (https://510kreport.com/company/id)

## Its most-cited devices
- K052738: Infusioncath Peripheral Infusion Catheter, Models VF0012, VF0016, VF0024, VF0028, VF0032, VF0036, VF0040, VF0044 (2005), cited by 1

## Recent decisions
- K073400: Varicath Peripheral Infusion Catheter (Dec 20, 2007)
- K052738: Infusioncath Peripheral Infusion Catheter, Models VF0012, VF0016, VF0024, VF0028, VF0032, VF0036, VF0040, VF0044 (Dec 6, 2005)

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