Kisco International is one of 291 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Kisco International - FDA 510(k) Cleared Devices
Recent clearances: ODALYS Pedicle Screw System
1
Total
1
Cleared
0
Denied
Kisco International has 1 FDA 510(k) cleared medical devices. Based in Saint-Priest, FR.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Kisco International Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Rich Jansen, Pharm.D. as regulatory consultant.
FDA 510(k) Regulatory Record - Kisco International
1 devices