# Myolyn, LLC

- Location (FDA's records): Gainesville, FL
- FDA decisions: 2 (2017–2022): 2 510(k) clearances
- Product codes: GZI (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Restorative Therapies, Inc.: 1 (https://510kreport.com/company/restorative-therapies)

## Its most-cited devices
- K170132: MyoCycle Home, MyoCycle Pro (2017), cited by 1

## Recent decisions
- K213925: MyoCycle MC-2 (Home / Home + / Pro / Pro +) (Apr 25, 2022)
- K170132: MyoCycle Home, MyoCycle Pro (Apr 25, 2017)

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