# Medphoton GmbH

- Location (FDA's records): Salzburg, AT
- FDA decisions: 4 (2016–2025): 4 510(k) clearances
- Product codes: OWB (2), IYE (2)
- 510(k) review time since 2016: median 143 days, against 90 for FDA's reviews in the same codes and years (1 of 4 faster)
- Predicates its devices cite: 5 (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
- Elekta, Ltd.: 1 (https://510kreport.com/company/elekta)
- Wfr/Aquaplast Corp.: 1 (https://510kreport.com/company/wfr-aquaplast)
- Ziehm Imaging GmbH: 1 (https://510kreport.com/company/ziehm-imaging)

## Its most-cited devices
- K161400: ImagingRing System (2016), cited by 1
- K203281: Mobile ImagingRing System, IRm, Loop-X Mobile Imaging Robot, Loop-X (2020), cited by 1

## Recent decisions
- K234067: ImagingRing m (Version 2.0); Loop-X (Version 2.0); Loop-X Mobile Imaging Robot (Version 2.0) (Mar 28, 2025)
- K203281: Mobile ImagingRing System, IRm, Loop-X Mobile Imaging Robot, Loop-X (Dec 22, 2020)
- K191267: ImagingRing System on Rails (Aug 1, 2019)
- K161400: ImagingRing System (Dec 8, 2016)

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