# Goosen Enterprises, Inc.

- Location (FDA's records): Goldenrod, FL
- FDA decisions: 4 (1985–1994): 4 510(k) clearances
- Product codes: EZD (1), GCX (1), GBP (1), KNX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K923848: Goosen Self-Lubricating Catheter (Feb 18, 1994)
- K896134: Acuflo, Vacuum-Powered Body Fluid Suction Appara. (Aug 30, 1990)
- K896579: Goosen Urinary Drainage System (Feb 15, 1990)
- K844889: Mensink-Goosen Catheter (Mar 18, 1985)

Source page: https://510kreport.com/company/goosen-enterprises