# Lifebridge Medizintechnik AG

- Location (FDA's records): Bryn Mawr, PA
- FDA decisions: 3 (2009–2011): 3 510(k) clearances
- Product codes: KFM (2), DTQ (1)
- Predicates its devices cite: 9 (2 its own); citations of its devices by later devices: 3 (2 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
- Avecor Cardiovascular, Inc.: 2 (https://510kreport.com/company/avecor-cardiovascular)
- Bard Cardiosurgery Div: 1 (https://510kreport.com/company/bard-cardiosurgery-div)
- Medtronic Perfusion Systems: 1 (https://510kreport.com/company/medtronic-perfusion-systems)
- Rand S.R.L.: 1 (https://510kreport.com/company/rand)
- Jostra AG: 1 (https://510kreport.com/company/jostra)
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)

## Firms that cite its devices most
- Maquet Cardiopulmonary, AG: 1 (https://510kreport.com/company/maquet-cardiopulmonary)

## Its most-cited devices
- K090006: Lifebridge B2T, Model 7001 (2009), cited by 3

## Recent decisions
- K111384: Lifebridge (May 24, 2011)
- K103357: Lifebridge (Dec 27, 2010)
- K090006: Lifebridge B2T, Model 7001 (Oct 15, 2009)

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