Kb Medical (Group), Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kb Medical (Group), Inc. - FDA 510(k) Cleared Devices
Recent clearances: Enteral Feeding Set
1
Total
1
Cleared
0
Denied
Kb Medical (Group), Inc. has 1 FDA 510(k) cleared medical devices. Based in Irvine, US.
Last cleared in 2021. Active since 2021. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Kb Medical (Group), Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mid-Link Consulting Co, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Kb Medical (Group), Inc.
1 devices