# Cardiomedical GmbH

- Location (FDA's records): Amsterdam, NL
- FDA decisions: 1 (2013–2013): 1 510(k) clearance
- Product codes: DXC (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (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
- American Edwards Laboratories: 2 (https://510kreport.com/company/american-edwards-laboratories)
- Microsurgical Laboratories,Inc.Dba Wexler Surgical: 1 (https://510kreport.com/company/microsurgical-laboratories-dba-wexler-surgical)

## Firms that cite its devices most
- Biorep Technologies, Inc.: 1 (https://510kreport.com/company/biorep-technologies)

## Its most-cited devices
- K123571: Cardio Vision Mics Aortic Clamps (2013), cited by 1

## Recent decisions
- K123571: Cardio Vision Mics Aortic Clamps (Aug 1, 2013)

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