# Meps, LLC

- Location (FDA's records): Fort Lauderdale, FL
- FDA decisions: 1 (2002–2002): 1 510(k) clearance
- Product codes: GWF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (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 that cite its devices most
- Axon Systems, Inc.: 2 (https://510kreport.com/company/axon-systems)
- Nihon Kohden Corporation: 1 (https://510kreport.com/company/nihon-kohden)
- Nihon Kohden America, Inc.: 1 (https://510kreport.com/company/nihon-kohden-america)
- Digitimer, Ltd.: 1 (https://510kreport.com/company/digitimer)

## Its most-cited devices
- K020400: Digitimer D185 Multipulse Cortical Stimulator (2002), cited by 5

## Recent decisions
- K020400: Digitimer D185 Multipulse Cortical Stimulator (Aug 23, 2002)

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