# Genicon, LC

- Location (FDA's records): Orlando, FL
- FDA decisions: 6 (1999–2003): 6 510(k) clearances
- Product codes: GCJ (3), HIF (1), FZP (1), GEA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 16 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Gynetech Pty., Ltd.: 1 (https://510kreport.com/company/gynetech)
- Unimax Medical Systems, Inc.: 1 (https://510kreport.com/company/unimax-medical-systems)

## Its most-cited devices
- K993625: Insufflation Needle- 120MM, Model 900-200 (2000), cited by 2

## Recent decisions
- K030174: Genicon Laparoscopes (Jun 19, 2003)
- K030269: Genicon Clip Applier (Mar 20, 2003)
- K002542: Reusable Cannula (Oct 23, 2000)
- K993625: Insufflation Needle- 120MM, Model 900-200 (Jun 20, 2000)
- K991382: Shieldedtrocar/Cannula System, Model 101-005-101 (Jul 15, 1999)
- K982472: Genicon Trocar (Feb 4, 1999)

Source page: https://510kreport.com/company/genicon-lc