# Sienco, Inc.

- Location (FDA's records): Boulder, CO
- FDA decisions: 5 (1995–2023): 5 510(k) clearances
- Product codes: JBP (4), JPA (1)
- Predicates its devices cite: 4 (4 its own); citations of its devices by later devices: 4 (4 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K952560: Sonoclot Coagulation & Platelet Function Analyzer (1995), cited by 3
- K002528: Sonoclot Coagulation & Platelet Function Analyzer System with Signature Viewer Option (2000), cited by 1

## Recent decisions
- K223635: Sonoclot Coagulation & Platelet Function Analyzer System with Sonoclot Viewer (Jan 4, 2023)
- K032952: Aiact Kit (Dec 12, 2003)
- K002528: Sonoclot Coagulation & Platelet Function Analyzer System with Signature Viewer Option (Aug 31, 2000)
- K984141: Gbact + Kit (May 28, 1999)
- K952560: Sonoclot Coagulation & Platelet Function Analyzer (Sep 5, 1995)

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