# Ventrex, Inc.

- Location (FDA's records): Ventura, CA
- FDA decisions: 6 (1992–2006): 6 510(k) clearances
- Names in FDA's records: Ventrex, Inc. (5); Ventrex, LLC (1)
- Product codes: DHB (2), HFM (2), CCL (1), DQA (1)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 4 (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
- Vascular Technology Incorporated: 1 (https://510kreport.com/company/vascular-technology)
- Seatronics Co.: 1 (https://510kreport.com/company/seatronics)
- Corometrics Medical Systems, Inc.: 1 (https://510kreport.com/company/corometrics-medical-systems)
- Hewlett-Packard Co.: 1 (https://510kreport.com/company/hewlett-packard)
- Ge Medical Systems Information Technologies: 1 (https://510kreport.com/company/ge-medical-systems-information-technologies)

## Firms that cite its devices most
- Clinical Innovations, Inc.: 1 (https://510kreport.com/company/clinical-innovations)
- Reproductive Research Technologies, LP: 1 (https://510kreport.com/company/reproductive-research-technologies)
- T F & G Products: 1 (https://510kreport.com/company/t-f-g-products)

## Its most-cited devices
- K013477: Toco Lite, Model TD-01 (2002), cited by 3
- K964821: Coverox Sheath Models Number PS65, PS67, EPS65 and EPS67 (1997), cited by 1

## Recent decisions
- K061044: Featherlite Aqua Tocodynamometer (Jul 12, 2006)
- K013477: Toco Lite, Model TD-01 (Jan 17, 2002)
- K964821: Coverox Sheath Models Number PS65, PS67, EPS65 and EPS67 (Jul 16, 1997)
- K963415: Ventrex Oxygen Sensor (Nov 25, 1996)
- K925044: Ventrex Allergen Disc (May 14, 1993)
- K924119: Ventrex Allergen Disc (Nov 30, 1992)

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