# Contour Technology

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 1 (2012–2012): 1 510(k) clearance
- Product codes: NGX (1)
- Predicates its devices cite: 3 (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)
- Valmed Corp.: 1 (https://510kreport.com/company/valmed)
- Bio-Medical Research, Ltd.: 1 (https://510kreport.com/company/bio-medical-research)

## Firms that cite its devices most
- Well Brain International, Ltd.: 2 (https://510kreport.com/company/well-brain-international)

## Its most-cited devices
- K111476: Contour Technology Muscle Stimulator (2012), cited by 2

## Recent decisions
- K111476: Contour Technology Muscle Stimulator (May 23, 2012)

Source page: https://510kreport.com/company/contour-technology