Vallum Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vallum Corporation - FDA 510(k) Cleared Devices
Recent clearances: Peekplus® Interbody Fusion Device
1
Total
1
Cleared
0
Denied
Vallum Corporation has 1 FDA 510(k) cleared medical devices. Based in Nashua, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Vallum Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by O'Connell Regulatory Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Vallum Corporation
1 devices