# Pfrimmer-Viggo GmbH & Co.

- Location (FDA's records): Washington, DC
- FDA decisions: 1 (1992–1992): 1 510(k) clearance
- Product codes: LEM (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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 that cite its devices most
- Integra LifeSciences Corporation: 1 (https://510kreport.com/company/integra-lifesciences)
- Cook Biotech, Inc.: 1 (https://510kreport.com/company/cook-biotech)

## Its most-cited devices
- K910555: Tutoplast Dura (1992), cited by 2

## Recent decisions
- K910555: Tutoplast Dura (Apr 20, 1992)

Source page: https://510kreport.com/company/pfrimmer-viggo