# Curatronic, Ltd.

- Location (FDA's records): Heshmonayim, IL
- FDA decisions: 2 (2005–2008): 2 510(k) clearances
- Product codes: IPF (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 2 (1 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
- Dan Med, Inc.: 1 (https://510kreport.com/company/dan-med)
- Danmeter A/S: 1 (https://510kreport.com/company/danmeter-a-s)

## Firms that cite its devices most
- Myomo, Inc.: 1 (https://510kreport.com/company/myomo)

## Its most-cited devices
- K042650: Biomove 3000 (2005), cited by 2

## Recent decisions
- K080787: Biomove 5000 System (Apr 17, 2008)
- K042650: Biomove 3000 (Jan 27, 2005)

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