Kalitec Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kalitec Medical - FDA 510(k) Cleared Devices
Recent clearances: NIDO™ Pedicle Screw System
1
Total
1
Cleared
0
Denied
Kalitec Medical has 1 FDA 510(k) cleared medical devices. Based in Orlando, US.
Last cleared in 2023. Active since 2023. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Kalitec Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MCRA as regulatory consultant.
FDA 510(k) Regulatory Record - Kalitec Medical
1 devices