Endocontrol is one of 289 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
2
Total
2
Cleared
0
Denied
Endocontrol has 2 FDA 510(k) cleared medical devices. Based in La Tronche, FR.
Historical record: 2 cleared submissions from 2008 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Endocontrol Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Endocontrol
2 devices