# K142047: EIDON

- Pathway: 510(k) (Traditional)
- Applicant: Centervue S.P.A.
- Decided: Nov 12, 2014 after 107 days
- Product code: MYC (Ophthalmoscope, Laser, Scanning)
- Device class: 2
- Regulation: 21 CFR 886.1570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K941234 (1995). 20 ancestors in all.
8 later devices descend from it; 4 cite it directly.
0 of 29 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K111988: Easyscan Model 1.2, I-Optics BV (2011) Summary page 6.
- K101935: Centervue Digital Retinography System, Centervue S.P.A. (2010) Summary page 6.

## Most influential descendants
- K180526: Eidon FA (2018), 2 descendants of its own
- K211328: Eidon FA, Eidon, Eidon AF, Eidon Uwfl (2021), 1 descendant of its own
- K192113: DRSplus (2019), 1 descendant of its own
- K150320: Compass (2015), 1 descendant of its own
- K241931: OcuMet Beacon  (OCUB100) (2025), 0 descendants of its own

## Indications for use
The CenterVue EIDON is intended for taking digital images of a human retina without the use of a mydriatic agent.

Source page: https://510kreport.com/device/K142047
Methodology: https://510kreport.com/methodology