# Kessel Medintim GmbH

- Location (FDA's records): Frankfurt, DE
- FDA decisions: 1 (2014–2014): 1 510(k) clearance
- Product codes: HDW (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (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
- Johnson & Johnson Produtos Profissionais Ltda.: 1 (https://510kreport.com/company/johnson-johnson-produtos-profissionais)

## Recent decisions
- K140305: Caya Contoured Diaphragm (Aug 26, 2014)

Source page: https://510kreport.com/company/kessel-medintim