Eos Imaging, Inc.
Eos Imaging, Inc. holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2016, with 2 FDA device recalls on record.
Top product codes for Eos Imaging, Inc.
FDA recalls by Eos Imaging, Inc.
- Z-1460-2015 — EOS, Digital radiography system used in general radiographic examinations.
- Z-2072-2012 — EOS X-ray Medical Diagnostic , X-ray Equipment System Digital Radiography used in general radiographic examination.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Eos Imaging, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.