# Distalmotion SA

- Location (FDA's records): Epalinges, CH
- FDA decisions: 5 (2024–2026): 4 510(k) clearances and 1 De Novo grant
- Product codes: SDD (5)
- Predicates its devices cite: 4 (4 its own); citations of its devices by later devices: 4 (4 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K251197: Dexter L6 System (2025), cited by 2
- DEN230084: Dexter L6 System (2024), cited by 2

## Recent decisions
- K261398: Dexter L6 System (Aug 11, 2026)
- K260653: Dexter L6 System (Jun 11, 2026)
- K251197: Dexter L6 System (Sep 30, 2025)
- K250435: Dexter L6 System (May 27, 2025)
- DEN230084: Dexter L6 System (Oct 25, 2024)

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