# Scandimed International

- Location (FDA's records): Jamestown, RI
- FDA decisions: 2 (2008–2009): 2 510(k) clearances
- Product codes: MND (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
- Scandimed. A.S.: 2 (https://510kreport.com/company/scandimed)

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

## Its most-cited devices
- K083556: Modification to Auto-Band Ligator (2009), cited by 1
- K081142: Auto-Band Ligator (2008), cited by 1

## Recent decisions
- K083556: Modification to Auto-Band Ligator (Feb 19, 2009)
- K081142: Auto-Band Ligator (May 16, 2008)

Source page: https://510kreport.com/company/scandimed-international