# Digitimer, Ltd.

- Location (FDA's records): Fort Lauderdale, FL
- FDA decisions: 2 (2005–2018): 2 510(k) clearances
- Product codes: GWF (1), IPF (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 6 (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
- Meps, LLC: 1 (https://510kreport.com/company/meps)
- Radionics, Inc.: 1 (https://510kreport.com/company/radionics)

## Firms that cite its devices most
- Nuvasive, Inc.: 3 (https://510kreport.com/company/nuvasive)
- Cadwell Industries, Inc.: 1 (https://510kreport.com/company/cadwell-industries)
- Tonica Elektronik A/S: 1 (https://510kreport.com/company/tonica-elektronik-a-s)
- Sunmed, Inc.: 1 (https://510kreport.com/company/sunmed)

## Its most-cited devices
- K051357: DS7A Constant Current High Voltage Stimulator, Model DS7A; DS7AH Constant Current High Voltage Stimulator, Model DS7AH (2005), cited by 5
- K172381: Digitimer DS7AP Constant Current Stimulator (2018), cited by 1

## Recent decisions
- K172381: Digitimer DS7AP Constant Current Stimulator (Mar 6, 2018)
- K051357: DS7A Constant Current High Voltage Stimulator, Model DS7A; DS7AH Constant Current High Voltage Stimulator, Model DS7AH (Sep 20, 2005)

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