# Micomed Ortho GmbH

- Location (FDA's records): Lake Forest, CA
- FDA decisions: 2 (2002–2003): 2 510(k) clearances
- Product codes: MNI (1), KWQ (1)
- Predicates its devices cite: 6 (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 whose devices it cites most
- Depuy, Inc.: 2 (https://510kreport.com/company/depuy)
- Medical Device Technologies, Inc.: 1 (https://510kreport.com/company/medical-device-technologies)
- Micomed GmbH: 1 (https://510kreport.com/company/micomed)
- Stuart Drug & Surgical Supply, Inc.: 1 (https://510kreport.com/company/stuart-drug-surgical-supply)
- Acromed Corp.: 1 (https://510kreport.com/company/acromed)

## Firms that cite its devices most
- Medicrea Technologies: 1 (https://510kreport.com/company/medicrea-technologies)

## Its most-cited devices
- K024125: Halm Zielke Instrumentation System (2003), cited by 1

## Recent decisions
- K024125: Halm Zielke Instrumentation System (Sep 22, 2003)
- K021275: Micomed Posterior Doublerod System (Jul 18, 2002)

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