# Myndtec, Inc.

- Location (FDA's records): Mississauga, CA
- FDA decisions: 3 (2017–2024): 3 510(k) clearances
- Product codes: GZI (3)
- Predicates its devices cite: 4 (3 its own); citations of its devices by later devices: 3 (3 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
- Bioness, Inc.: 1 (https://510kreport.com/company/bioness)

## Its most-cited devices
- K170564: MyndMove System, MyndMove Functional Electrical Stimulator (2017), cited by 2
- K212149: MyndMove 2.0 (2022), cited by 1

## Recent decisions
- K233006: MyndMove, MyndMove 2.0 (Jun 25, 2024)
- K212149: MyndMove 2.0 (Mar 3, 2022)
- K170564: MyndMove System, MyndMove Functional Electrical Stimulator (Aug 30, 2017)

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