Ecleris USA is one of 16129 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ecleris USA - FDA 510(k) Cleared Devices
Recent clearances: ECLERIS SINUSCOPE, ECLERIS MICROSTAR COLPOSCOPE
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: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Ecleris USA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ecleris USA
2 devices