# Micomed GmbH

- Location (FDA's records): Fullerton, CA
- FDA decisions: 2 (1999–2000): 2 510(k) clearances
- Product codes: MNI (1), KWQ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Micomed Ortho GmbH: 1 (https://510kreport.com/company/micomed-ortho)

## Its most-cited devices
- K982006: Micomed - Halm Zielke Instrumentation (1999), cited by 1

## Recent decisions
- K991862: Micomed Posterior Doublerod System (MPDS) (Jan 13, 2000)
- K982006: Micomed - Halm Zielke Instrumentation (Jan 20, 1999)

Source page: https://510kreport.com/company/micomed