# Thermopeutix, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 5 (2008–2013): 5 510(k) clearances
- Product codes: MJN (3), DQY (2)
- Predicates its devices cite: 7 (3 its own); citations of its devices by later devices: 6 (3 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
- Origen Biomedical, Inc.: 1 (https://510kreport.com/company/origen-biomedical)
- Coaxia, Inc.: 1 (https://510kreport.com/company/coaxia)
- Estech, Inc.: 1 (https://510kreport.com/company/estech)
- MicroVention, Inc.: 1 (https://510kreport.com/company/microvention)

## Firms that cite its devices most
- Tractus Vascular, LLC: 2 (https://510kreport.com/company/tractus-vascular)
- Renovorx, Inc.: 1 (https://510kreport.com/company/renovorx)

## Its most-cited devices
- K080700: Duoflo Catheter (2008), cited by 2
- K132701: Primi Support Catheter (2013), cited by 2
- K130850: Primi and Secondi Support Catheters (2013), cited by 1
- K112219: Tapas Catheter (2011), cited by 1

## Recent decisions
- K132701: Primi Support Catheter (Sep 26, 2013)
- K130850: Primi and Secondi Support Catheters (Jun 25, 2013)
- K112219: Tapas Catheter (Nov 18, 2011)
- K093847: Duflo Catheter (Heparin Coated) (Aug 25, 2010)
- K080700: Duoflo Catheter (Sep 26, 2008)

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