# Scanditronix Medical AB

- Location (FDA's records): Uppsala S-754 50, SE
- FDA decisions: 4 (1997–2001): 4 510(k) clearances
- Product codes: IYE (4)
- Predicates its devices cite: 6 (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
- Scanditronix, Inc.: 4 (https://510kreport.com/company/scanditronix)
- Medical Physics Instrumentation, Inc.: 1 (https://510kreport.com/company/medical-physics-instrumentation)

## Firms that cite its devices most
- Iba Dosimetry GmbH: 1 (https://510kreport.com/company/iba-dosimetry)

## Its most-cited devices
- K011763: Omnidos (2001), cited by 1
- K961400: Rfa-300, Lda Utility (1997), cited by 1

## Recent decisions
- K011763: Omnidos (Sep 5, 2001)
- K002051: Invidos (Sep 5, 2000)
- K990734: DPD-12PCC (May 28, 1999)
- K961400: Rfa-300, Lda Utility (Jan 3, 1997)

Source page: https://510kreport.com/company/scanditronix-medical