# Xentek Medical, Inc.

- Location (FDA's records): Athens, TX
- FDA decisions: 2 (2000–2000): 2 510(k) clearances
- Product codes: DRE (1), DYB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 9 (0 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Galt Medical Corp.: 6 (https://510kreport.com/company/galt-medical)
- Martech Medical Products, Inc.: 1 (https://510kreport.com/company/martech-medical-products)
- Arrow International, Inc. (Subsidiary of Teleflex, Inc.): 1 (https://510kreport.com/company/arrow-international-subsidiary-of-teleflex)
- Vascular Solutions, Inc.: 1 (https://510kreport.com/company/vascular-solutions)

## Its most-cited devices
- K000313: Tearaway Introducer Sheath (2000), cited by 6
- K000737: Coaxial Dilator Set (2000), cited by 3

## Recent decisions
- K000737: Coaxial Dilator Set (Aug 1, 2000)
- K000313: Tearaway Introducer Sheath (Jun 16, 2000)

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