# Eos Imaging

- Location (FDA's records): Paris, FR
- FDA decisions: 17 (2012–2025): 17 510(k) clearances
- Names in FDA's records: Eos Imaging (15); Eos Imaging, Inc. (2)
- Product codes: LLZ (6), KPR (5), QIH (4), MQB (2)
- 510(k) review time since 2016: median 117 days, against 141 for FDA's reviews in the same codes and years (5 of 10 faster)
- Predicates its devices cite: 25 (16 its own); citations of its devices by later devices: 18 (16 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Biospace Med: 8 (https://510kreport.com/company/biospace-med)
- Onefit Medical: 1 (https://510kreport.com/company/onefit-medical)

## Firms that cite its devices most
- Corin USA: 1 (https://510kreport.com/company/corin-usa)
- Mighty Oak Medical, Inc.: 1 (https://510kreport.com/company/mighty-oak-medical)

## Its most-cited devices
- K172346: sterEOS Workstation (2018), cited by 3
- K240582: VEA Align; spineEOS (2024), cited by 2
- K251747: VEA Align; spineEOS (2025), cited by 1
- K130395: Stereos Workstation (2013), cited by 1
- K142773: EOS System (2015), cited by 1
- K160914: sterEOS Workstation (2016), cited by 1

## Recent decisions
- K251078: AutoDensity (Nov 14, 2025)
- K251747: VEA Align; spineEOS (Aug 15, 2025)
- K233920: EOSedge (Aug 6, 2024)
- K240582: VEA Align; spineEOS (Jun 25, 2024)
- K231917: VEA Align (Jan 5, 2024)
- K232086: spineEOS (Oct 24, 2023)
- K202394: EOSedge (Sep 16, 2020)
- K192079: EOSedge (Nov 27, 2019)

Source page: https://510kreport.com/company/eos-imaging