# Ndd Medizintechnik AG

- Location (FDA's records): Zurich, CH
- FDA decisions: 4 (2017–2023): 4 510(k) clearances
- Product codes: BZG (2), CAH (1), BTY (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ndd Medizitechnik AG: 2 (https://510kreport.com/company/ndd-medizitechnik)
- Ndd Medical Technologies: 1 (https://510kreport.com/company/ndd-medical-technologies)
- A-M Systems, Inc.: 1 (https://510kreport.com/company/a-m-systems)

## Firms that cite its devices most
- Vitalograph (Ireland), Ltd.: 1 (https://510kreport.com/company/vitalograph-ireland)

## Its most-cited devices
- K161536: EasyOne Air Spirometer (2017), cited by 1
- K161534: EasyOne Pro Respiratory Analysis System (2017), cited by 1

## Recent decisions
- K230178: EasyOne Sky Spirometer (Oct 19, 2023)
- K221250: EasyOne Filter (Nov 22, 2022)
- K161534: EasyOne Pro Respiratory Analysis System (Feb 22, 2017)
- K161536: EasyOne Air Spirometer (Jan 5, 2017)

Source page: https://510kreport.com/company/ndd-medizintechnik