# Toul Meditech AB

- Location (FDA's records): Vasteras, SE
- FDA decisions: 3 (2016–2019): 3 510(k) clearances
- Product codes: ORC (3)
- 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
- STERIS Corporation: 1 (https://510kreport.com/company/steris)
- Nimbic Systems, Inc.: 1 (https://510kreport.com/company/nimbic-systems)

## Firms that cite its devices most
- Surgicube International B.V.: 1 (https://510kreport.com/company/surgicube-international)

## Its most-cited devices
- K153498: Operio (2016), cited by 2

## Recent decisions
- K190027: SteriStay (May 10, 2019)
- K173349: Operio (Dec 20, 2017)
- K153498: Operio (Jul 20, 2016)

Source page: https://510kreport.com/company/toul-meditech