# Origen Biomedical, Inc.

- Location (FDA's records): Austin, TX
- FDA decisions: 4 (2001–2012): 4 510(k) clearances
- Product codes: LPZ (1), DQO (1), DWF (1), DWC (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 16 (9 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Janus Biomedical, Inc.: 1 (https://510kreport.com/company/janus-biomedical)

## Firms that cite its devices most
- Thermopeutix, Inc.: 1 (https://510kreport.com/company/thermopeutix)
- Avalon Laboratories, LLC: 1 (https://510kreport.com/company/avalon-laboratories)
- Kerberos Proximal Solutions, Inc.: 1 (https://510kreport.com/company/kerberos-proximal-solutions)

## Its most-cited devices
- K003288: Origen Dual Lumen Catheter (2001), cited by 3

## Recent decisions
- K113869: Origen Reinforced Dual Lumen Catheter (Jul 26, 2012)
- K021702: Cryobag, Model CB (Aug 6, 2002)
- K003288: Origen Dual Lumen Catheter (Jun 8, 2001)
- K003145: Origen Bladder Holder (Apr 20, 2001)

Source page: https://510kreport.com/company/origen-biomedical