# Endothelix, Inc.

- Location (FDA's records): Houston, TX
- FDA decisions: 2 (2007–2007): 2 510(k) clearances
- Product codes: DQK (2)
- Predicates its devices cite: 4 (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

## Firms whose devices it cites most
- Vivant Medical, Inc.: 1 (https://510kreport.com/company/vivant-medical)
- Endocare, Inc.: 1 (https://510kreport.com/company/endocare)
- Uri Therm-X, Inc.: 1 (https://510kreport.com/company/uri-therm-x)
- Itamar Medical, Ltd.: 1 (https://510kreport.com/company/itamar-medical)

## Recent decisions
- K072919: Vendys, Model 6000 B B/C (Nov 2, 2007)
- K060980: Vendys Model 5000 B/BC (Aug 16, 2007)

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