Velmeni, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Velmeni, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Velmeni for Dentists (V4D) Endo-Perio, VELMENI for DENTISTS (V4D), Velmeni for Dentists (V4D)
4
Total
4
Cleared
0
Denied
Velmeni, Inc. has 4 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Latest FDA clearance: Jul 2026. Active since 2024. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Velmeni, Inc. Filter by specialty or product code using the sidebar.
1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
FDA 510(k) Regulatory Record - Velmeni, Inc.
4 devices