# Venocare, Inc.

- Location (FDA's records): Doral, FL
- FDA decisions: 3 (2025–2026): 3 510(k) clearances
- Product codes: FOZ (2), JKA (1)
- 510(k) review time since 2016: median 203 days, against 115 for FDA's reviews in the same codes and years (0 of 3 faster)
- 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
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Becton Dickinson Infusion Therapy Systems, Inc.: 1 (https://510kreport.com/company/becton-dickinson-infusion-therapy-systems)

## Its most-cited devices
- K243105: Ruby Intravascular Catheter (2025), cited by 1

## Recent decisions
- K260432: Ruby Intravascular Catheter (Sep 2, 2026)
- K244047: Navi™ Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG) (May 23, 2025)
- K243105: Ruby Intravascular Catheter (May 16, 2025)

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