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