Endobionics, Inc. is one of 24542 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endobionics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ENDOBIONICS MICROSYRINGE (USYRINGE) INFUSION CATHETER
1
Total
1
Cleared
0
Denied
Endobionics, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Leandro, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Endobionics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kema Quality B.V. as regulatory consultant.
FDA 510(k) Regulatory Record - Endobionics, Inc.
1 devices