# Cyberkinetics, Inc. (Cki)

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 1 (2005–2005): 1 510(k) clearance
- Product codes: GZL (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Cyberkinetics Neurotechnology Systems, Inc.: 1 (https://510kreport.com/company/cyberkinetics-neurotechnology-systems)
- Ad-Tech Medical Instrument Corp: 1 (https://510kreport.com/company/ad-tech-medical-instrument)

## Its most-cited devices
- K042384: Neuroport Recording Microelectrode Array System (2005), cited by 2

## Recent decisions
- K042384: Neuroport Recording Microelectrode Array System (Mar 29, 2005)

Source page: https://510kreport.com/company/cyberkinetics-cki
