# Coviden, LLC

- Location (FDA's records): Boulder, CO
- FDA decisions: 1 (2017–2017): 1 510(k) clearance
- Product codes: NEY (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
- Covidien: 2 (https://510kreport.com/company/covidien)

## Firms that cite its devices most
- Covidien: 2 (https://510kreport.com/company/covidien)

## Its most-cited devices
- K171358: Emprint SX Ablation Platform and Accessories (2017), cited by 2

## Recent decisions
- K171358: Emprint SX Ablation Platform and Accessories (Sep 1, 2017)

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