# Idmed

- Location (FDA's records): Marseille, FR
- FDA decisions: 3 (2018–2025): 3 510(k) clearances
- Product codes: KOI (2), BSK (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 3 (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
- Hamilton Medical AG: 1 (https://510kreport.com/company/hamilton-medical)
- Organon Teknika Corp.: 1 (https://510kreport.com/company/organon-teknika)

## Firms that cite its devices most
- Senzime AB: 1 (https://510kreport.com/company/senzime)
- Nerbio Medical Software Platforms, Inc.: 1 (https://510kreport.com/company/nerbio-medical-software-platforms)

## Its most-cited devices
- K172690: ToFscan (2018), cited by 3

## Recent decisions
- K243562: CuffGuard (Aug 12, 2025)
- K243339: WiTOF (Jun 23, 2025)
- K172690: ToFscan (May 31, 2018)

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