# Seigla Medical, Inc.

- Location (FDA's records): Buffalo, MN
- FDA decisions: 2 (2022–2025): 2 510(k) clearances
- Product codes: DQY (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 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
- Vascular Solutions, Inc.: 1 (https://510kreport.com/company/vascular-solutions)

## Its most-cited devices
- K220691: LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension (2022), cited by 1

## Recent decisions
- K243691: LiquID .051 LP Guide Catheter Extension (Apr 4, 2025)
- K220691: LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension (May 5, 2022)

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