# Par Medizintechnik GmbH & Co. KG

- Location (FDA's records): Berlin, DE
- FDA decisions: 2 (2001–2017): 2 510(k) clearances
- Names in FDA's records: Par Medizintechnik GmbH & Co. KG (1); Par Medizintechnik GmbH (1)
- Product codes: DXN (2)
- Predicates its devices cite: 2 (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
- Industrielle Entwicklung Medizintechnik Und Vertri: 1 (https://510kreport.com/company/industrielle-entwicklung-medizintechnik-und-vertri)

## Firms that cite its devices most
- Biotrac, Inc.: 1 (https://510kreport.com/company/biotrac)

## Its most-cited devices
- K012647: Tonoport V (2001), cited by 2

## Recent decisions
- K170966: Tonoport VI (Jun 14, 2017)
- K012647: Tonoport V (Nov 9, 2001)

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