# Cionic

- Location (FDA's records): San Francisco, CA
- FDA decisions: 3 (2022–2025): 3 510(k) clearances
- Names in FDA's records: Cionic (2); Cionic, Inc. (1)
- Product codes: GZI (3)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 2 (2 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
- Otto Bock, Austria GmbH: 1 (https://510kreport.com/company/otto-bock-austria)
- Bioness, Inc.: 1 (https://510kreport.com/company/bioness)

## Its most-cited devices
- K213622: Cionic Neural Sleeve NS-100 (2022), cited by 1
- K221823: Cionic Neural Sleeve NS-100 (2022), cited by 1

## Recent decisions
- K243828: Cionic Neural Sleeve (NS-200) (May 2, 2025)
- K221823: Cionic Neural Sleeve NS-100 (Jul 21, 2022)
- K213622: Cionic Neural Sleeve NS-100 (Feb 14, 2022)

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