# Domino S.R.L.

- Location (FDA's records): West Hartford, CT
- FDA decisions: 2 (2007–2007): 2 510(k) clearances
- Product codes: NGX (1), IPF (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (0 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
- Compex S.A.: 1 (https://510kreport.com/company/compex)
- Chattanooga Group, Inc.: 1 (https://510kreport.com/company/chattanooga-group)

## Firms that cite its devices most
- Chattanooga Group, Inc.: 2 (https://510kreport.com/company/chattanooga-group)

## Its most-cited devices
- K061632: Globus Premium Muscle Stimulator (2007), cited by 1
- K071431: Globus Genesy 1100 Stimulator (2007), cited by 1

## Recent decisions
- K071431: Globus Genesy 1100 Stimulator (Sep 21, 2007)
- K061632: Globus Premium Muscle Stimulator (Apr 30, 2007)

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