# Dan Med, Inc.

- Location (FDA's records): Denver, CO
- FDA decisions: 6 (1997–2002): 6 510(k) clearances
- Product codes: IPF (4), GZJ (1), KPI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 8 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Hollister, Inc.: 2 (https://510kreport.com/company/hollister)
- Ness-Neuromuscular Electrical Stimulation Systems: 1 (https://510kreport.com/company/ness-neuromuscular-electrical-stimulation-systems)
- Curatronic, Ltd.: 1 (https://510kreport.com/company/curatronic)
- Cole & Associates: 1 (https://510kreport.com/company/cole-associates)
- Chattanooga Group, Inc.: 1 (https://510kreport.com/company/chattanooga-group)
- Thought Technology, Ltd.: 1 (https://510kreport.com/company/thought-technology)
- Care Rehab and Orthopaedic: 1 (https://510kreport.com/company/care-rehab-and-orthopaedic)

## Its most-cited devices
- K972997: AM800 Automove Emg Triggered Electrical Muscle Stimulation (1997), cited by 4
- K012885: Neuromove NM900 (2001), cited by 2
- K964738: Elpha 2000 Conti (1997), cited by 2

## Recent decisions
- K013210: Truwave (Apr 4, 2002)
- K012885: Neuromove NM900 (Nov 8, 2001)
- K010745: EMS 3000 (Jun 27, 2001)
- K991241: IF8000 (Nov 2, 1999)
- K972997: AM800 Automove Emg Triggered Electrical Muscle Stimulation (Nov 10, 1997)
- K964738: Elpha 2000 Conti (Aug 14, 1997)

Source page: https://510kreport.com/company/dan-med