Kdi Med Supply is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kdi Med Supply - FDA 510(k) Cleared Devices
Recent clearances: 3 Ply Medical Grade Single Use Procedural Disposable Face Mask
1
Total
1
Cleared
0
Denied
Kdi Med Supply has 1 FDA 510(k) cleared medical devices. Based in Fremont, US.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Kdi Med Supply Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Kdi Med Supply
1 devices