# Miegmbh

- Location (FDA's records): Seth, DE
- FDA decisions: 4 (2010–2020): 4 510(k) clearances
- Product codes: KPS (4)
- Predicates its devices cite: 11 (2 its own); citations of its devices by later devices: 2 (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
- Cti Pet Systems, Inc.: 4 (https://510kreport.com/company/cti-pet-systems)
- Medical Imaging Electronics America, Inc.: 1 (https://510kreport.com/company/medical-imaging-electronics-america)
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)
- Siemens Gammasonics, Inc.: 1 (https://510kreport.com/company/siemens-gammasonics)
- Invia: 1 (https://510kreport.com/company/invia)
- Siemens Corp.: 1 (https://510kreport.com/company/siemens)

## Its most-cited devices
- K130269: Ecat Scintron Pet (2013), cited by 1
- K101013: Modification to Scintron IV (2010), cited by 1

## Recent decisions
- K201807: Ancoris (Aug 27, 2020)
- K130269: Ecat Scintron Pet (Apr 19, 2013)
- K101768: Mie Scintron Gamma Camera Systems (Oct 5, 2010)
- K101013: Modification to Scintron IV (Jun 7, 2010)

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