# Scanmed, LLC

- Location (FDA's records): Omaha, NE
- FDA decisions: 1 (2022–2022): 1 510(k) clearance
- Product codes: QDQ (1)
- Predicates its devices cite: 1 (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
- Screenpoint Medical B.V.: 1 (https://510kreport.com/company/screenpoint-medical)

## Firms that cite its devices most
- Quibim S.L.: 1 (https://510kreport.com/company/quibim)
- Quantib B.V.: 1 (https://510kreport.com/company/quantib)

## Its most-cited devices
- K212783: ProstatID (2022), cited by 2

## Recent decisions
- K212783: ProstatID (Jul 8, 2022)

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