# Vertex Medical Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 21 (1982–1984): 21 510(k) clearances
- Product codes: DXT (7), DQO (6), DYB (1), DQX (1), FMI (1), DYG (1), LJE (1), DRE (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
- K833742: Eschmann Dilation Catheter (Apr 24, 1984)
- K834476: Nephrostomy/Biliary Drainage Bag (Feb 4, 1984)
- K832380: Protective Sleeve (Nov 28, 1983)
- K831666: Sialography Needle (Jul 12, 1983)
- K830576: Lymphangiography Set (Mar 17, 1983)
- K830420: Polyethylene Monitoring Connectors (Feb 28, 1983)
- K830237: Translucent Poly. Cath. Connector and (Feb 18, 1983)
- K823190: Backstop Valve W/Side Arm (Dec 30, 1982)

Source page: https://510kreport.com/company/vertex-medical