Kalitec Medical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kalitec Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: Navagio Lumbar Cage, TiWAVE-L Porous Titanium Lumbar Cage
2
Total
2
Cleared
0
Denied
Kalitec Medical, LLC has 2 FDA 510(k) cleared medical devices. Based in Orlando, US.
Last cleared in 2022. Active since 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Kalitec Medical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by The OrthoMedix Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Kalitec Medical, LLC
2 devices