Ecleris USA is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ecleris USA - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Ecleris USA has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 2 cleared submissions from 2010 to 2014. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Ecleris USA Filter by specialty or product code using the sidebar.
Ecleris USA — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jun 09, 2014
ECLERIS SINUSCOPE
Ear, Nose, Throat
397d
Cleared
Jul 09, 2010
ECLERIS MICROSTAR COLPOSCOPE
Obstetrics & Gynecology
129d