# Alcyone Lifesciences, Inc.

- Location (FDA's records): Lowell, MA
- FDA decisions: 2 (2015–2017): 2 510(k) clearances
- Product codes: JXG (1), HCD (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
- Integra Neurosciences Implants S.A.: 1 (https://510kreport.com/company/integra-neurosciences-implants)
- Surgivision, Inc.: 1 (https://510kreport.com/company/surgivision)

## Firms that cite its devices most
- Parker Hannifin Corp.: 1 (https://510kreport.com/company/parker-hannifin)
- Anuncia Medical, Inc.: 1 (https://510kreport.com/company/anuncia-medical)

## Its most-cited devices
- K172006: Alivio Ventricular Catheter and Flusher System (Alivio System) (2017), cited by 1
- K150660: Alcyone MEMS Cannula (AMC) System (2015), cited by 1

## Recent decisions
- K172006: Alivio Ventricular Catheter and Flusher System (Alivio System) (Nov 9, 2017)
- K150660: Alcyone MEMS Cannula (AMC) System (Apr 16, 2015)

Source page: https://510kreport.com/company/alcyone-lifesciences