# Dura Tap, LLC

- Location (FDA's records): Wayne, PA
- FDA decisions: 2 (2018–2018): 2 510(k) clearances
- Product codes: GAW (1), NBY (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (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
- Riverpoint Medical: 2 (https://510kreport.com/company/riverpoint-medical)

## Firms that cite its devices most
- Antarma, LLC Dba Golnit Sutures: 1 (https://510kreport.com/company/antarma-dba-golnit-sutures)
- Durastat, LLC: 1 (https://510kreport.com/company/durastat)

## Its most-cited devices
- K173335: Gazelle PTFE and Suture Delivery Device (2018), cited by 2

## Recent decisions
- K173644: Gazelle Polypropylene Suture and Delivery Device (Feb 15, 2018)
- K173335: Gazelle PTFE and Suture Delivery Device (Feb 8, 2018)

Source page: https://510kreport.com/company/dura-tap